- Quarterly Report (10-Q)

Share Name	Share Symbol	Market	Type
Bio Bridge Science Inc (CE)	USOTC:BGES	OTCMarkets	Common Stock

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

WASHINGTON, D.C. 20549

FORM 10-Q

x QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15( d ) OF THE SECURITIES EXCHANGE

ACT OF 1934

For the quarterly period ended: September 30, 2010

¨ TRANSITION REPORT PURSUANT TO SECTION 13 0R 15( d ) OF THE SECURITIES EXCHANGE

ACT OF 1934

For the transition period from _______ to _______

Commission File Number: 000-51497

BIO-BRIDGE SCIENCE, INC.

(Exact name of small business issuer as specified in its charter)

Del aware	20-1802936
(State or other jurisdiction of incorporation or organization)	(IRS Employer Identification No.)

1801 South Meyers Road , Suite 220, Oakb rook Terrace , Illinois, 60 181

(Address of principal executive offices, Zip Code)

( 630 ) 613-9687

(Issuer's telephone number including area code)

Check whether the issuer (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days: Yes x No ¨

Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, or a smaller reporting company. See the definitions of “large accelerated filer,” “accelerated filer” and “smaller reporting company” in Rule 12b-2 of the Exchange Act.

Large accelerated filer	¨	Accelerated filer ¨
Non-accelerated filer	¨ (Do not check if a smaller reporting company)	Smaller reporting company x

Indicate by check mark whether the registrant is a shell company: Yes ¨ No x

State the number of shares outstanding of each of the issuer's classes of common stock, as of the latest practicable date.

45,070,245

Number of Shares of Common Stock, Par Value $0.001 Per Share, Outstanding as of September 30, 2010

BIO-BRIDGE SCIENCE, INC.

FORM 10-Q

TABLE OF CONTENTS

		Page
PART I.	FINANCIAL INFORMATION

Item 1.	Financial Statements

	Condensed Consolidated Balance Sheets as of September 30, 2010 (Unaudited) and December 31, 2009	2

	Unaudited Condensed Consolidated Statements of Operations for the three and nine months ended September 30, 2010 and 2009	3

	Unaudited Condensed Consolidated Statements of Changes in Equity for the nine months ended September 30, 2010	4

	Unaudited Condensed Consolidated Statements of Cash Flows for the nine months ended September 30, 2010 and 2009	5

	Notes to the Unaudited Condensed Consolidated Financial Statements	6

Item 2.	Management's Discussion and Analysis of Financial Conditions and Results of Operation	13

Item 3.	Quantitative and Qualitative Disclosure About Market Risk	19

Item 4.	Controls and Procedures	19

PART II.	OTHER INFORMATION

Item 1.	Legal Proceedings	20

Item 1A.	Risk Factors	20

Item 2.	Unregistered Sales of Equity Securities and Use of Proceeds	20

Item 3.	Defaults Upon Senior Securities	20

Item 4.	Submission of Matters to a Vote of Security Holders	20

Item 5.	Other Information	20

Item 6.	Exhibits	20

SIGNATURES		20

EXHIBIT INDEX		21

PART I - FINANCIAL INFORMATION

Item 1. Financial Statements

BIO-BRIDGE SCIENCE, INC. AND SUBSIDIARIES

CONDENSED CONSOLIDATED BALANCE SHEETS

	September 30,			December 31,
	20 10			200 9
	(Unaudited)
ASSETS
Current Assets
Cash and cash equivalents	$	568,188		$	1,481,851
Accounts receivable, net		209,128			471,236
Inventories		864,741			589,730
Trading securities, at fair value		-			162,044
Prepaid expenses and other current assets		123,015			62,663
Total Current Assets		1,765,072			2,767,524

Property and equipment, net		3,402,999			3,465,302
Land use right, net		512,352			522,510
Intangible assets		223,844			219,677
Goodwill		-			243,248
Other long-term assets		3,825			-
Total Long-term Assets		4,143,020			4,450,737

TOTAL ASSETS	$	5,908,092		$	7,218,261

LIABILITIES AND EQUITY
Current Liabilities
Accounts payable	$	185,908		$	161,122
Accrued expenses and other payables		110,979			144,795
Payable for leasehold and equipment purchases		-			273,558
Payable to contractors		-			42,471
Due to director		22,242			15,183
Advances from director		300,000			-
Derivative liabilities		185,315			377,013
Total Current Liabilities		804,444			1,014,142

Equity
Preferred stock, $0.001 par value, 5,000,000 shares authorized, 0 and 4,000,000 shares issued and outstanding, respectively		-			4,000
Common stock, $0.001 par value, 100,000,000 shares authorized, 45,070,245 and 40,819,285 shares issued and outstanding, respectively		45,070			40,819
Additional paid-in capital		18,433,694			16,475,947
Preferred stock dividend, payable in common shares		-			74,200
Subscription receivable		(210,325	)		(210,325	)
Stock to be issued		210,000			248,140
Accumulated other comprehensive income		367,028			261,948
Accumulated deficit		(14,585,265	)		(11,678,908	)
Total Bio-Bridge Science, Inc. Shareholders’ Equity		4,260,202			5,215,821

NONCONTROLLING INTERESTS		843,446			988,298

Total Equity		5,103,648			6,204,119

TOTAL LIABILITIES AND EQUITY	$	5,908,092		$	7, 218 ,261

See accompanying notes to the condensed consolidated financial statements

BIO-BRIDGE SCIENCE, INC. AND SUBSIDIARIES

CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS

(Unaudited)

	Three Months Ended September 30,						Nine Months Ended September 30,
	2010			2009			2010			2009

Revenue	$	102,852		$	142,901		$	310,693		$	582,925
Cost of goods sold		(57,810	)		(92,052	)		(203,952	)		(376,780	)
Gross profit		45,042			50,849			106,741			206,145

Research and development costs		38,898			69,308			171,764			148,960
Selling and distribution expenses		29,094			57,619			97,498			148,581
General and administrative expenses		308,589			308,704			2,647,960			808,109

Loss from operations		(331,539	)		(384,782	)		(2,810,481	)		(899,505	)

Other income (expense):
Interest expense		(2,226	)		(340	)		(5,294	)		(637	)
Unrealized gain on trading securities		-			21,779			6,741			40,965
Gain on sale of trading securities		-			-			1,890			-
Change of fair value of derivative liability		10,752			(958,147	)		15,665			268,271
Dividend income		-			3,612			4,718			11,719
Impairment of goodwill		(243,248	)		-			(243,248	)		-

Loss before income taxes		(566,261	)		(1,317,878	)		(3,030,009	)		(579,187	)

Benefit (provision) for income taxes		-			2,199			-			(15,552	)

Net Loss		(566,261	)		(1,315,679	)		(3,030,009	)		(594,739	)

Net income (loss) attributable to noncontrolling interests		(43,105	)		(3,005	)		(144,852	)		23,701

Net loss attributable to Bio-Bridge Science, Inc.		(523,156	)		(1,312,674	)		(2,885,157	)		(618,440	)

Preferred stock dividends		-			(94,650	)		(21,200	)		(339,400	)

Net loss attributable to common shareholders	$	(523,156	)	$	(1,407,324	)	$	(2,906,357	)	$	(957,840	)

Net loss per share, attributable to common shareholders, basic and diluted	$	(0.01	)	$	(0.04	)	$	(0.07	)	$	(0.03	)

Weighted average shares outstanding, basic and diluted		45,070,245			35,199,705			44,582,497			35,116,833

See accompanying notes to the condensed consolidated financial statements

BIO-BRIDGE SCIENCE, INC. AND SUBSIDIARIES

CONDENSED CONSOLIDATED STATEMENTS OF CHANGES IN EQUITY

For The Nine Months Ended September 30, 2010

(Unaudited)

	Common Stock				Preferred Stock						Preferred Stock Dividend Payable in			Additional Paid-in		Accumulated Other Comprehensive		Common Stock To			Subscription			Accumulated			Non controlling
	Shares		Amount		Shares			Amount			Common Shares			Capital		Income		Be Issued			Receivable			Deficit			Interest			Total
BALANCE December 31, 2009		40,819,285	$	40,819		4,000,000		$	4,000		$	74,200		$	16,475,947	$	261,948	$	248,140		$	(210,325	)	$	(11,678,908	)	$	988,298		$	6,204,119

Accrual of preferred stock dividend		-		-		-			-			21,200			-		-		-			-			(21,200	)		-			-

Payment of preferred stock dividend through issuance of common stock		180,000		180		-			-			(95,400	)		95,220		-		-			-			-			-			-

Fair value of vested options		-		-		-			-			-			126,621		-		-			-			-			-			126,621

Fair value of warrants issued to directors		-		-		-			-			-			1,521,805		-		-			-			-			-			1,521,805

Issuance of common shares		70,960		71		-			-			-			38,069		-		(38,140	)		-			-			-			-

Extinguishment of derivative recorded as contribution to capital		-		-		-			-			-			176,032		-		-			-			-			-			176,032

Conversion of 4,000,000 shares of preferred stock into 4,000,000 shares of common stock		4,000,000		4,000		(4,000,000	)		(4,000	)		-			-		-		-			-			-			-			-

Foreign currency translation gain		-		-		-			-			-			-		105,080		-			-			-			-			105,080

Net Loss		-		-		-			-			-			-		-		-			-			(2,885,157	)		(144,852	)		(3,030,009	)

BALANCE September 30, 2010 (Unaudited)		45,070,245	$	45,070		-		$	-		$	-		$	18, 433,694	$	367,028	$	210,000		$	(210,325	)	$	(14,585,265	)	$	843,446		$	5,103,648

See accompanying notes to the condensed consolidated financial statements

BIO-BRIDGE SCIENCE, INC. AND SUBSIDIARIES

CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS

(Unaudited)

	Nine Months Ended September 30
	20 10			200 9
CASH FLOWS FROM OPERATING ACTIVITIES
Net loss	$	(3,030,009	)	$	(594,739	)
Adjustments to reconcile net loss to net cash used in operating activities:
Depreciation		309,179			73,002
Amortization of land use right		10,158			14,044
Fair value of vested options		126,621			71,863
Fair value of warrants issued to directors		1,521,805			-
Fair value of common stock issued to employees		-			9,540
Gain on sale of trading securities		(1,890	)		-
Unrealized gain on trading securities		(6,741	)		(40,965	)
Change in fair value of derivative liability		(15,666	)		(268,271	)
Impairment of goodwill		243,248			-
Change in operating assets and liabilities:
Accounts receivable		262,108			(32,140	)
Inventories		(275,011	)		(98,452	)
Prepaid expense and other assets		(60,352	)		101
Accounts payable		24,786			(28,733	)
Accrued expenses and other payables		(33,816	)		(88,319	)
Payable to contractors		(42,471	)		-
Net cash used in operating activities		(968,051	)		(983,069	)

CASH FLOWS FROM INVESTING ACTIVITIES
Paid security deposit for office lease		(3,825	)		-
Increase in construction in progress		-			(24,537	)
Purchase of property and equipment		(251,043	)		(362,058	)
Payable for leasehold and equipment purchases		(273,558	)		-
Payable to contractors for construction in progress		-			(141,288	)
Proceeds from sale of trading securities		170,675			-
Net cash used in investing activities		(357,751	)		(527,883	)

CASH FLOWS FROM FINANCING ACTIVITIES
Proceeds from issuance of common stock		-			1,869,945
Advances from director		300,000
Due to (from) director		7,059			(18,198	)
Net cash provided by financing activities		307,059			1,851,747

NET (DECREASE) INCREASE IN CASH AND CASH EQUIVALENTS		(1,018,743	)		340,795

Effect of exchange rate changes on cash		105,080			1,342
Cash and cash equivalents, beginning of period		1,481,851			1,486,252

CASH AND CASH EQUIVALENTS, END OF PERIOD	$	568,188		$	1,828,389

SUPPLEMENTAL CASH FLOW INFORMATION
Income taxes paid	$	-		$	49,425

SUPPLEMENTAL NON-CASH FLOW INVESTING AND FINANCING ACTIVITIES
Conversion of shares of preferred stock into shares of common stock	$	4,000		$	-
Extinguishment of derivative recorded as contribution to capital	$	176,032		$	-
Accrual of preferred stock dividend payable in common stock	$	21,200		$	339,400
Payment of preferred stock dividend in shares of common stock	$	95,400		$	450,000

See accompanying notes to the condensed consolidated financial statements

BIO-BRIDGE SCIENCE, INC. AND SUBSIDIARIES

NOTES TO THE UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

AS OF SEPTEMBER 30, 2010

NOTE 1 - BASIS OF PRESENTATION

The accompanying unaudited condensed consolidated financial statements of Bio Bridge Science Inc. and Subsidiaries (the "Company") have been prepared in accordance with accounting principles generally accepted in the United States of America for interim financial information and pursuant to the requirements for reporting on Form 10-Q and Regulation S-K for scaled disclosures for smaller reporting companies. Accordingly, they do not include all the information and footnotes required by accounting principles generally accepted in the United States of America for complete financial statements. However, such information reflects all adjustments (consisting solely of normal recurring adjustments), which are, in the opinion of management, necessary for the fair presentation of the consolidated financial position and the consolidated results of operations. Results shown for interim periods are not necessarily indicative of the results to be obtained for a full fiscal year.

The condensed consolidated balance sheet information as of December 31, 2009 was derived from the audited consolidated financial statements included in the Company's Annual Report on Form 10-K filed with the SEC on March 31, 2010. These interim financial statements should be read in conjunction with that report.

NOTE 2 - ORGANIZATION AND PRINCIPAL ACTIVITIES

Bio-Bridge Science, Inc (the “Company") was incorporated in the State of Delaware on October 26, 2004. The Company's fiscal year end is December 31. On December 1, 2004, the Company acquired all of the outstanding shares of Bio-Bridge Science Corporation ("BBS"), a Cayman Islands corporation, in exchange for 29,971,590 shares of its common stock, and as a result, BBS became a wholly owned subsidiary of Bio-Bridge Science, Inc. The acquisition was accounted for as a reverse merger (recapitalization) with BBS deemed to be the accounting acquirer, and the Company the legal acquirer.

BBS was incorporated in the Cayman Islands on February 11, 2002. At the time of the exchange, BBS held a 100% interest in Bio-Bridge Science (Beijing) Corp. ("Bio-Bridge Beijing"), a wholly-foreign funded enterprise of the People's Republic of China ("PRC") which was established on May 20, 2002. Bio Bridge Beijing is currently engaged in the development and commercialization of several vaccine candidates in the PRC, such as HIV-PV vaccine I, cervical cancer vaccine, and colon cancer vaccine.

On July 31, 2008, the Company acquired 51 percent of the outstanding capital interest of Bio-Bridge Xinheng Baide Biotechnology Co., Ltd. (“Bio-Bridge XBB”). The primary operations of Bio-Bridge XBB are the manufacturing and distribution of bovine serum products, which are used in research and production of pharmaceuticals and veterinary medicines.

In June of 2009, the Company entered into an equity joint venture contract to purchase 51 percent of Bio-Bridge JRS Biosciences (Beijing) Co., Ltd. (“Bio-Bridge JRS”). On October 16, 2009 the joint venture received a business license to do business in the PRC and began its startup activities.

Going Concern

The accompanying consolidated financial statements have been prepared on a going concern basis, which contemplates the realization of assets and the settlement of liabilities and commitments in the normal course of business. As reflected in the accompanying consolidated financial statements, the Company had a net loss of $3,030,009 and used cash in operations of $968,051 for the nine months ended September 30, 2010, and had an accumulated deficit of $14,585,265 as of September 30, 2010. These factors raise substantial doubt about the Company’s ability to continue as a going concern, which is dependent upon the Company’s ability to raise additional funds to implement its business plan. The consolidated financial statements do not include any adjustments that might be necessary if the Company is unable to continue as a going concern.

Based on our current operating plan, we believe that we have sufficient cash and cash equivalents to last approximately through July 2011. We will need to obtain additional financing in addition to the funds already raised through the sale of equity securities to fund our cash needs and continue our operations beyond July 2011. Additional financing, whether through public or private equity or debt financing, arrangements with stockholders or other sources to fund operations, may not be available, or if available, may be on terms unacceptable to us. Our ability to maintain sufficient liquidity is dependent on our ability to raise additional capital. If we issue additional equity securities to raise funds, the ownership percentage of our existing stockholders would be reduced. New investors may demand rights, preferences or privileges senior to those of existing holders of our common stock. Debt incurred by us would be senior to equity in the ability of debt holders to make claims on our assets. The terms of any debt issued could impose restrictions on our operations. If adequate funds are not available to satisfy either medium or long-term capital requirements, our operations and liquidity could be materially adversely affected and we could be forced to cut back our operations.

NOTE 3 - SUMMARY OF PRINCIPAL ACCOUNTING POLICIES

Principles of Consolidation

The accompanying consolidated financial statements include the accounts of Bio-Bridge Science Inc. and our wholly owned subsidiaries, Bio-Bridge Science Corp., Bio-Bridge Beijing, Bio-Bridge Science Holding Co., Bio-Bridge Science (HK), Co. and our 51% owned subsidiaries Bio-Bridge XBB and Bio-Bridge JRS. Intercompany accounts and transactions have been eliminated in consolidation.

Use of Estimates

The preparation of financial statements in conformity with accounting principles generally accepted in the United States of America requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financial statements and the reported amounts of revenues and expenses during the reporting periods. Management makes these estimates using the best information available and the best judgment at the time the estimates are made, however actual results could differ materially from those estimates.

Revenue Recognition

The Company recognizes revenue from the sales of products in accordance with Securities and Exchange Commission (“SEC”) Staff Accounting Bulletin ("SAB") No. 104, when persuasive evidence of an order arrangement exists, delivery has occurred, the sales price is fixed or determinable and collectibility is reasonably assured. Generally, these criteria are met at the time the product is shipped to customers when title and risk of loss have transferred.

Accounts receivables are recognized and carried at original invoiced amount less an allowance for any uncollectible accounts. The Company uses the aging method to estimate the valuation allowance for anticipated uncollectible receivable balances. Under the aging method, bad debts determined by management are based on historical experience as well as the current economic climate and are applied to customers' balances categorized by the number of months the underlying invoices have remained outstanding. The valuation allowance balance is adjusted to the amount computed as a result of the aging method. When facts subsequently become available to indicate that an adjustment to the allowance should be made, this is recorded as a change in estimate in the current year. As of September 30, 2010 and December 31, 2009, accounts receivable were net of allowances of $52,230 and $40,037, respectively.

Goodwill

As required by guidance issued by the Financial Accounting Standards Board (“FASB”), management performs impairment tests of goodwill whenever an event occurs or circumstances change that indicate impairment has more likely than not occurred. Also, management performs impairment testing of goodwill at least annually.

Goodwill is related to the Company's acquisition of Bio-Bridge XBB (“XBB”) on July 31, 2008. Goodwill and other intangible assets are accounted for in accordance with guidance issued by the FASB on goodwill and other intangible assets. Under this guidance, goodwill is not amortized. Rather, goodwill is assessed for impairment at least annually. The Company tests goodwill by using a two-step process. In the first step, the fair value of the reporting unit is compared with the carrying amount of the reporting unit, including goodwill. If the carrying amount of the reporting unit exceeds its fair value, goodwill is considered impaired and a second step is performed to measure the amount of impairment loss, if any.

Factors that we consider important that could trigger an impairment review include significant underperformance relative to historical or projected future operating results, significant changes in the manner or use of our asset or the strategy for our overall business, and significant negative industry or economic trends. Based on management’s assessment, the market for XBB’s bovine serum is deteriorating in China. As such, the Company is currently under negotiation with a third party for the sale of its interest in XBB. At this stage of negotiation, it became evident that the recorded value of the goodwill to the XBB segment was impaired, and the Company’s management recorded an impairment of goodwill at September 30, 2010 of $243,248. There were no impairments of goodwill in 2009. Once an impairment of goodwill has been recorded, it cannot be reversed.

Intangible Assets

As required by guidance issued by the FASB, management performs impairment tests of indefinite-lived intangible assets whenever an event occurs or circumstances change that indicate impairment has more likely than not occurred. Also, management performs impairment testing indefinite-lived intangible assets at least annually.

Intangible assets subject to amortization are related to technology for producing cell culture medium contributed to Bio-Bridge JRS by a noncontrolling interest. In accordance with guidance issued by the FASB on accounting for the impairment and disposal of long-lived assets, the Company reviews intangible assets subject to amortization at least annually to determine if any adverse conditions exist or a change in circumstances has occurred that would indicate impairment or a change in the remaining useful life. If the carrying value of an asset exceeds its undiscounted cash flows, the Company writes down the carrying value of the intangible asset to its fair value in the period identified. If the carrying value of assets is determined not to be recoverable, the Company records an impairment loss equal to the excess of the carrying value over the fair value of the assets. The Company’s estimate of fair value is based on the best information available, in the absence of quoted market prices. The Company generally calculates fair value as the present value of estimated future cash flows that the Company expects to generate from the asset using a discounted cash flow income approach as described above. If the estimate of an intangible asset’s remaining useful life is changed, the Company amortizes the remaining carrying value of the intangible asset prospectively over the revised remaining useful life. Based on management’s assessment, there were no indications of impairment or change in the remaining useful life of recorded intangible assets at September 30, 2010.

Impairment of Long-Lived Assets

Authoritative guidance issued by the FASB establishes guidelines regarding when impairment losses on long-lived assets, which include property and equipment, should be recognized, and how impairment losses should be measured.

Management regularly reviews property, equipment and other long-lived assets for possible impairment. This review occurs quarterly, or more frequently if events or changes in circumstances indicate the carrying amount of the asset may not be recoverable. If there is indication of impairment, then management prepares an estimate of future cash flows (undiscounted and without interest charges) expected to result from the use of the asset and its eventual disposition. If these cash flows are less than the carrying amount of the asset, an impairment loss is recognized to write down the asset to its estimated fair value. Management’s assumptions about cash flows and discount rates require significant judgment. Factors we consider important that could trigger an impairment review include significant underperformance relative to historical or projected future operating results, significant changes in the manner of the use of our assets or the strategy for our overall business, and significant negative industry or economic trends. There were no indications of impairment based on management’s assessment at September 30, 2010.

Derivative Financial Instruments

The Company evaluates all of its financial instruments to determine if such instruments are derivatives or contain features that qualify as embedded derivatives. For derivative financial instruments that are accounted for as liabilities, the derivative instrument is initially recorded at its fair value and is then re-valued at each reporting date, with changes in the fair value reported in the condensed consolidated statements of operations. For stock-based derivative financial instruments, the Company uses the Black-Scholes-Merton option pricing models to value the derivative instruments at inception and on subsequent valuation dates. The classification of derivative instruments, including whether such instruments should be recorded as liabilities or as equity, is evaluated at the end of each reporting period.

Financial Assets and Liabilities Measured at Fair Value.

The Company reports fair value measurements in accordance with authoritative guidance issued by the FASB. Fair value is defined in the authoritative guidance as the price that would be received to sell an asset or paid to transfer a liability in the principal or most advantageous market for the asset or liability in an orderly transaction between market participants at the measurement date. A fair value hierarchy was established, which prioritizes the inputs used in measuring fair value into three broad levels as follows:

Level 1—Quoted prices in active markets for identical assets or liabilities.

Level 2—Inputs, other than the quoted prices in active markets, are observable either directly or indirectly.

Level 3—Unobservable inputs based on the Company's assumptions.

The Company is required to use observable market data if such data is available without undue cost and effort.

The following table presents certain investments and liabilities of the Company’s financial assets measured and recorded at fair value on the Company’s consolidated balance sheets on a recurring basis and their level within the fair value hierarchy as of September 30, 2010:

	Level 1		Level 2		Level 3		Total
Fair value of options and warrants	$	-	$	-	$	185,315	$	185,315
	$	-	$	-	$	185,315	$	185,315

Foreign Currency Translation

The accompanying consolidated financial statements are presented in United States dollars. The functional currency of the Company is the Renminbi (RMB). Equity accounts of the consolidated financial statements are translated into United States dollars from RMB at their historical exchange rates when the equity transactions occurred. Assets and liabilities are translated at the exchange rates as of balance sheet date. Income and expenditures are translated at the average of the exchange rates at beginning of the financial year and at balance sheet date.

	2010		2009
US$ to RMB exchange rate on January 1		6.8282		6.8346

US$ to RMB exchange rate on September 30		6.7011		6.8290

Average US$ to RMB exchange rate for the nine months ended September 30		6.8164		6.8318

The RMB is not freely convertible into foreign currency and all foreign exchange transactions must take place through authorized institutions. No representation is made that the RMB amounts could have been, or could be, converted into US dollars at the rates used in translation.

Comprehensive Income

Comprehensive income is defined to include all changes in equity except those resulting from investments by owners and distributions to owners. The Company’s current components of comprehensive income consist of foreign currency translation adjustments:

	Three months ended September 30								Nine months ended September 30
	2010				2009				2010				2009
Net loss attributable to Bio-Bridge Science, Inc.		$	(523,156	)		$	(1,312,674	)		$	(2,885,157	)		$	(618,440	)
Foreign currency translation gain			74,703				1,970				105,080				1,341
Comprehensive loss		$	(448,453	)		$	(1,310,704	)		$	(2,780,077	)		$	(617,099	)

Research and Development

Research and development costs are expensed as incurred. For the three months ended September 30, 2010 and 2009, research and development expenses totaled $38,898 and $69,308, respectively. For the nine months ended September 30, 2010 and 2009, research and development expenses totaled $171,764 and $148,960, respectively.

Loss Per Share

Basic loss per share is computed by dividing net loss attributable to Bio-Bridge Science, Inc.’s common shareholders by the weighted average number of common shares outstanding during the period. The diluted earnings per share calculation gives effect to all potentially dilutive common shares outstanding during the period using the treasury stock method. Common equivalent shares consist of shares issuable upon the exercise of stock options or warrants. As of September 30, 2010, common stock equivalents were composed of options convertible into 3,287,000 shares of the Company's common stock and warrants convertible into 8,814,943 shares of the Company's common stock. For the three and nine month periods ended September 30, 2010, respectively, common equivalent shares have been excluded from the calculation of loss per share as their effect is anti-dilutive.

Stock-Based Compensation

The Company periodically issues stock options and warrants to employees and non-employees in capital raising transactions, for services and for financing costs. Stock-based compensation is measured at the grant date, based on the fair value of the award, and is recognized as expense over the requisite service period. Options vest and expire according to terms established at the grant date. For the three and nine month periods ended September 30, 2010, stock-based compensation totaled $32,977 and $126,621, respectively.

Concentrations

Financial instruments, which potentially subject the Company to concentrations of credit risk, consist principally of cash and unsecured trade accounts receivable.

Cash denominated in Renminbi (“RMB”) with a US dollar equivalent of $418,866 and $1,258,137 at September 30, 2010 and December 31, 2009, respectively, was held in accounts at financial institutions located in the PRC. In addition, the Company maintains funds in bank accounts in the US which at times may exceed the federally insured balance of $250,000. The Company and its subsidiaries have not experienced any losses in such accounts and do not believe the cash is exposed to any significant risk.

For the three and nine months ended September 30, 2010, approximately 74% and 76%, respectively, of the Company’s sales were to customers located in China, compared to approximately 86% and 91% for the three and nine months ended September 30, 2009, respectively. For the nine months ended September 30, 2010, three customers accounted for 47% of total sales (23%, 14%, and 10%, respectively). At September 30, 2010, four customers accounted for 82% of accounts receivable (33%, 26%, 12%, and 11%, respectively).

Advances from Director

During the three months ended June 30, 2010, one of the Company’s directors advanced $300,000 to the Company in anticipation of making an equity investment. The terms of the equity investment are currently being negotiated as of the date of the issuance of this 10-Q. The advances are non-interest bearing, unsecured, and due on demand.

Recent Accounting Pronouncements

In April 2010, the Financial Accounting Standard Board (FASB) issued new accounting guidance to clarify that an employee share-based payment award with an exercise price denominated in the currency of a market in which a substantial portion of the entity's equity securities trades should not be considered to contain a condition that is not a market, performance, or service condition. Therefore, an entity would not classify such an award as a liability if it otherwise qualifies as equity. The amendments are effective for fiscal years, and interim periods within those fiscal years, beginning on or after December 15, 2010. The Company does not expect adoption of this standard will have an effect on our consolidated results of operation or our financial position.

In April 2010, the FASB issued new accounting guidance in applying the milestone method of revenue recognition to research or development arrangements. Under this guidance management may recognize revenue contingent upon the achievement of a milestone in its entirety, in the period in which the milestone is achieved, only if the milestone meets all the criteria within the guidance to be considered substantive. This standard is effective on a prospective basis for research and development milestones achieved in fiscal years, beginning on or after June 15, 2010. Early adoption is permitted; however, adoption of this guidance as of a date other than January 1, 2011 will require the Company to apply this guidance retrospectively effective as of January 1, 2010 and will require disclosure of the effect of this guidance as applied to all previously reported interim periods in the fiscal year of adoption. As the Company plans to implement this standard prospectively, the effect of this guidance will be limited to future transactions. The Company does not expect adoption of this standard to have a material impact on its financial position or results of operations as it has no material research and development arrangements which will be accounted for under the milestone method.

In January 2010, the FASB issued new accounting guidance which requires new disclosures regarding transfers in and out of Level 1 and Level 2 fair value measurements, as well as requiring presentation on a gross basis of information about purchases, sales, issuances and settlements in Level 3 fair value measurements. The guidance also clarifies existing disclosures regarding level of disaggregation, inputs and valuation techniques. The new guidance is effective for interim and annual reporting periods beginning after December 15, 2009. Disclosures about purchases, sales, issuances and settlements in the roll forward of activity in Level 3 fair value measurements are effective for fiscal years beginning after December 15, 2010. As this guidance requires only additional disclosure, there should be no impact on the consolidated financial statements of the Company upon adoption.

In October 2009, a new accounting consensus was issued for multiple-deliverable revenue arrangements. This consensus amends existing revenue recognition accounting standards. This consensus provides accounting principles and application guidance on whether multiple deliverables exist, how the arrangement should be separated and the consideration allocated. This guidance eliminates the requirement to establish the fair value of undelivered products and services and instead provides for separate revenue recognition based upon management’s estimate of the selling price for an undelivered item when there is no other means to determine the fair value of that undelivered item. Previously the existing accounting consensus required that the fair value of the undelivered item be the price of the item either sold in a separate transaction between unrelated third parties or the price charged for each item when the item is sold separately by the vendor. Under the existing accounting consensus, if the fair value of all of the elements in the arrangement was not determinable, then revenue was deferred until all of the items were delivered or fair value was determined. This new approach is effective prospectively for revenue arrangements entered into or materially modified in fiscal years beginning on or after June 15, 2010. The Company is in the process of evaluating whether the adoption of this standard will have a material effect on its financial position, results of operations or cash flows.

Other recent accounting pronouncements issued by the FASB (including its Emerging Issues Task Force), the AICPA, and the Securities Exchange Commission (the "SEC") did not or are not believed by management to have a material impact on the Company's present or future consolidated financial statements.

NOTE 4 - INVENTORIES

Inventories consist of the following at:

	September 30, 2010			December 31, 2009
	(Unaudited)
Raw materials		$	269,358		$	205,968
Finished goods			595,383			383,762
Total inventories		$	864,741		$	589,730

NOTE 5 - EQUITY

Preferred Stock

On December 31, 2006, the Company amended its certificate of incorporation to provide for 5,000,000 shares of Series A preferred stock. Pursuant to the Company's certificate of incorporation, its board of directors has the authority, without further action by the stockholders, to issue up to 5,000,000 shares of undesignated preferred stock, par value $0.001 per share. The Company's board had the authority, without the approval of the stockholders, to fix the designations, powers, preferences, privileges and relative, participating, optional or special rights and the qualifications, limitations or restrictions of any preferred stock issued, including dividend rights, conversion rights, voting rights, terms of redemption and liquidation preferences, any or all of which may be greater than the rights of the common stock. Preferred stock could thus be issued with terms that could delay or prevent a change in control of our company or make removal of management more difficult.

In 2007, the Company sold 4,000,000 shares of Series A Convertible Preferred Stock with warrants to purchase 3,000,000 shares of common stock for $0.75 per unit, or $3,000,000 in aggregate. The preferred stock earned dividends at 12% annually, in common shares of the Company valued at $1.00 per share, payable semiannually in arrears. The preferred stock dividend was cumulative and non-participating.

The 3,000,000 warrants issued with the preferred stock in 2007 expired on January 30, 2010. Also on January 30, 2010, holders of 4,000,000 shares of the Company’s convertible preferred stock elected to convert the preferred shares into shares of the Company’s common stock on a one-for-one basis. Effective January 30, 2010, the preferred shares were converted, common shares were issued, and the accrual of the preferred stock dividend was discontinued. (See Note 7)

NOTE 6 - STOCK OPTION AND WARRANTS

At September 30, 2010, stock options outstanding were as follows:

	Number of Options			Weighted Average Exercise Price
Outstanding at January 1, 2010		3,731,500		$	0.45

Granted		-			-
Exercised		-			-
Forfeited		(444,500	)		(0.01	)

Outstanding at September 30, 2010		3,287,000		$	0.44

The following table summarizes information about stock options outstanding as of September 30, 2010:

Options Outstanding					Options Exercisable
Range of Exercise Prices	Number of Shares		Weighted Average Exercise Price		Weighted Average Remaining Contractual Life (in years)	Number of Shares		Weighted Average Exercise Price
$0.001 to $0.55		3,287,000	$	0.44	6.04		2,950,296	$	0.44

Information relating to stock options at September 30, 2010 summarized by exercise price is as follows:

	Option Outstanding				Options Exercisable
	Exercise price	Number of shares		Remaining life (years)	Exercise price		Number of Shares		Weighted average exercise price
$	0.001		400,000	5.33	$	0.001		400,000	$	0.00
$	0.001		20,000	1.75	$	0.001		20,000	$	0.00
$	0.001		3,000	8.80	$	0.001		3,000	$	0.00
$	0.47		540,000	8.80	$	0.47		378,081	$	0.06
$	0.50		1,207,000	5.25	$	0.50		1,207,000	$	0.21
$	0.52		240,000	8.80	$	0.52		131,970	$	0.02
$	0.55		600,000	5.33	$	0.55		600,000	$	0.11
$	0.50		277,000	9.22	$	0.50		210,245	$	0.04
$	0.001 to 0.55		3,287,000	1.75 to 9.22	$	0.45		2,950,296	$	0.44

The aggregate intrinsic value of 3,287,000 options outstanding and 2,950,296 options exercisable as of September 30, 2010 were $303,087 and $290,289, respectively. The aggregate intrinsic value for the options is calculated as the difference between the price of the underlying awards and quoted price of the Company’s common shares for the options that were in-the-money as of September 30, 2010.

Common Stock Warrants

On January 20, 2010, Company issued warrants to three companies controlled by two directors to purchase 3,000,000 shares of common stock at $1.00 per share with a term of five years. We recorded the fair value of the warrants to purchase 3,000,000 shares of common stock as compensation cost. The fair value of five-year warrant issued to these three companies was $1,521,805 at the grant date, which was determined using the Black-Scholes-Merton valuation method, using the following assumptions: no expected dividend yield; a risk-free interest rate of 1.62%; an expected life of 5 years; and an estimated volatility of 191 percent based on recent history of the stock price in the industry. The total of $1,521,805 was charged to compensation cost at the date the warrants were granted.

At September 30, 2010, warrants outstanding were as follows:

	Number of Shares Under Warrants			Weighted Average Exercise Price
Warrants outstanding at January 1, 2010		8,814,943		$	0.95
Warrants granted		3,000,000		$	1.00
Warrants expired		(3,000,000	)	$	1.00
Warrants outstanding and exercisable at September 30, 2010		8,814,943		$	0.95

The following table summarizes information about warrants outstanding at September 30, 2010:

Warrants Outstanding and Exercisable
Number of Shares Under Warrants	Exercise Price		Expiration Date	Weighted Average Exercise Price
183,334	$	0.75	June 4, 2011	$	0.02
183,333	$	1.20	June 4, 2013	$	0.02
1,724,138	$	0.725	July 2, 2012	$	0.14
1,724,138	$	1.10	July 2, 2013	$	0.22
1,000,000	$	0.725	July 9, 2012	$	0.08
1,000,000	$	1.10	July 9, 2013	$	0.12
3,000,000	$	1.00	January 20, 2015	$	0.34
8,814,943	$	0.75 to 1.20		$	0.95

There was no aggregate intrinsic value of 8,814,943 warrants outstanding and exercisable as of September 30, 2010 based on the trading price as of the period then ended.

NOTE 7 – DERIVATIVE LIABILITY

The strike price of options and warrants issued by the Company, and the conversion feature in the Company’s preferred stock previously outstanding, are denominated in US dollars, a currency other than the Company’s functional currency, RMB. Under authoritative guidance issued by the FASB these instruments are not considered indexed to the Company’s own stock and therefore the fair value of certain of the Company’s options and warrants, and the conversion feature of the preferred stock previously outstanding, are characterized as derivative liabilities. The FASB’s guidance requires the fair value of these liabilities be re-measured at the end of every reporting period with the change in value reported in the statement of operations.

At September 30, 2010, the Company had 3,287,000 options and 8,814,943 warrants outstanding. The Company determined that 3,167,000 of the options and 8,488,276 of the warrants were issued pursuant to share-based payments and therefore were not subject to the liability accounting.

At September 30, 2010 and December 31, 2009, the derivative liabilities were valued using the Black-Scholes-Merton valuation technique with the following assumptions:

	September 30, 2010			December 31, 2009

Risk-free interest rate		0.26	%		1.62	%
Expected volatility		207.6	%		191.0	%
Expected life (in years)	1 to 2.6 years			1 to 3 years
Expected dividend yield		0.00	%		0.00	%

Fair Value:
Options and warrants	$	185,315		$	235,877
Conversion feature		-			141,136
	$	185,315		$	377,013

The risk-free interest rate is based on the yield available on U.S. Treasury securities. The Company estimates volatility based on the historical volatility if its common stock. The expected life of the options and warrants and conversion feature are based on the expiration date of the related options and warrants and convertible preferred stock. The expected dividend yield was based on the fact that the Company has not paid dividends to common shareholders in the past and does not expect to pay dividends to common shareholders in the future.

At December 31, 2009, the Company recorded a total derivative liability of $377,013. Included in this total was $176,032 related to warrants issued with preferred stock and the conversion feature of the preferred stock. When the preferred stock was converted and related warrants expired (see Note 5), the derivative liability of $176,032 was extinguished and recorded as a contribution to capital. For the three months ended September 30, 2010 and 2009, change in derivative liability was $10,752 and $(958,147), respectively. For the nine months ended September 30, 2010 and 2009, change in derivative liability was $15,665 and $268,271, respectively.

Item 2. Management's Discussion and Analysis of Financial Condition and Results of Operation

Some of the statements made by us in this Quarterly Report on Form 10-Q are forward-looking in nature, including but not limited to, statements relating to our future revenue and expenses, product development, future market acceptance, levels of research and development, our management's plans and objectives for our current and future operations, and other statements that are not historical facts. Forward-looking statements include, but are not limited to, statements that are not historical facts, and statements including forms of the words "intend", "believe", "will", "may", "could", "expect", "anticipate", "plan", "possible", and similar terms. Actual results could differ materially from the results implied by the forward looking statements due to a variety of factors, many of which are discussed throughout this Quarterly Report and in our SEC filings. Readers are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date hereof. We undertake no obligation to publicly release any revisions to these forward-looking statements that may reflect events or circumstances after the date hereof or to reflect the occurrence of unanticipated events, unless required by law. Factors that could cause actual results to differ materially from those expressed in any forward-looking statement made by us include, but are not limited to:

o	our ability to finance our activities and maintain our financial liquidity;

o	our ability to attract and retain qualified, knowledgeable employees;

o	our ability to complete product development;

o	our ability to obtain regulatory approvals to conduct clinical trials;

o	our ability to design and market new products successfully;

o	our failure to acquire new customers in the future;

o	deterioration of business and economic conditions in our markets; and

o	intensely competitive industry conditions.

In this document, the words "we," "our," "ours," and "us" refers to Bio-Bridge Science, Inc. and our wholly owned subsidiaries, including Bio-Bridge Science (Beijing) Co. Ltd., a Wholly-Foreign Owned Enterprise of the People's Republic of China ("Bio-Bridge Beijing"), Bio-Bridge Science Corporation, a Cayman Islands corporation, Bio-Bridge Science Holding Co. Ltd, a Cayman Islands corporation, Bio-Bridge Science(HK) CO. Ltd, a Hong Kong company, Bio-Bridge Xinheng Baide Biotechnology Co. Ltd. (“Bio-Bridge XBB”), a Chinese company, and Bio-Bridge JRS Biosciences (Beijing) Co., Ltd (“Bio-Bridge JRS”), a Chinese company.

OVERVIEW

Bio-Bridge Science, Inc. is a biotechnology company whose subsidiaries are focused on the commercial development of HIV-PV Vaccine I, HPV vaccine, colon cancer vaccine, mucosal adjuvant and manufacture and sales of vaccine production-related materials. Bio-Bridge Beijing is conducting our vaccine development, Bio-Bridge XBB sells bovine serum, and Bio-Bridge JRS is producing powdered cell culture medium for sales in the near future.

Our primary corporate focus is on the commercial development of our potential vaccine products through our subsidiaries. Our capital requirements, particularly as they relate to product research and development, have been and will continue to be significant. Our future cash requirements and the adequacy of available funds will depend on many factors, including the pace at which we are able to obtain regulatory approvals of vaccine candidates, whether or not a market develops for our products and, if a market develops, the pace at which it develops, and the pace at which the technology involved in making our products changes.

Plans of Operation

Vaccine Development

The vaccine development is being undertaken by our 100% owned subsidiary, BBS Beijing. The pre-clinical testing of HIV-PV Vaccine I on laboratory animals was completed by the Beijing Institute of Radiation Medicine in June 2006 and showed encouraging results. To produce the HIV vaccine for clinical trials, we have built a GMP-compliant facility in Beijing. We have purchased and installed the laboratory equipment and the facility is operating well. Our HIV vaccine is being produced and quality control procedures are being established to meet SFDA standards. Pending the availability of funds and upon the completion of our preparatory procedures, we plan to apply to China's State Food and Drug Administration for approval to conduct clinical trials of HIV-PV Vaccine I. The clinical trial for preventive vaccine will last five to seven years.

We also plan to conduct the pre-clinical trials for colon cancer vaccine and HPV vaccine. We estimate that we will begin the pre-clinical trial of colon cancer vaccine and that of HPV vaccine when funding is available. We expect to enter clinical trials of colon cancer vaccine and HPV vaccine pending satisfactory results of the pre-clinical trials and the availability of funds. The clinical trial for therapeutic vaccine is expected to last three years. All the technology to make HIV vaccine and colon cancer vaccine is based on the technology co-developed by our CEO, Dr. Liang Qiao. Because we use the same technology to develop our potential vaccine products, we expect to use the same GMP facility in Beijing, China, to produce the HIV vaccine and colon cancer vaccine for pre-clinical and clinical trials.

To date we have run our operations from funds we raised in private offerings. During the next twelve months, we will need to raise capital through an offering of our securities, or from loans, to continue research and development of our various vaccine product candidates in China as well as conducting potential acquisition activities in China. We estimate that our capital requirements for the next twelve months will be as follows:

o	approximately $1.25 million for working capital and general corporate needs;

o	approximately $0.5 million for HIV vaccine Phase I clinical trial and its preparatory work;

o	approximately $1.0 million for pre-clinical trials on colon cancer vaccine and HPV vaccine.

We expect that the therapeutic vaccine can be brought to market in three years and the preventive vaccine can be brought to market in five to seven years after SFDA approval of clinical trials on these vaccines, depending on raising funds to complete development of the vaccines. As of September 30, 2010, our cash and cash equivalents was $568,188. Although we raised capital in 2008 and 2009 in private placements, we will still need to raise additional funds through the public or private sales of our securities, taking loans, or a combination of the foregoing to meet our planned operations. We cannot guarantee that financing will be available to us, on acceptable terms or at all. We also may borrow from local banks in China given that our land use rights and laboratory facility could be used as collateral for borrowing. If we fail to obtain other financing in the next 12 months, either through an offering of our securities or by obtaining additional loans, we may be unable to develop our planned projects as scheduled and may be forced to scale back.

Distribution of Xinhua Surgical Instruments

We signed an exclusive agency agreement with Xinhua Surgical Instruments Co. Ltd. (“Xinhua”) to distribute its products in the United States at the end of 2005. The agreement was superseded by a new agreement signed with Xinhua on March 17, 2008. The March 17, 2008 agreement has been amended on several occasions, with the most recent amendment on December 9, 2009. Under the most recent terms of the agreement, we have been granted exclusive distribution rights for all Xinhua surgical instruments in the United States, Australia, New Zealand and Costa Rica. Our minimum order placement requirement for these four areas in the first year calculated from the signing date will be $55,000 and increases by 10% over the previous year’s minimum order placement annually thereafter. We are responsible for advertising and marketing expenses in connection with distribution of Xinhua surgical instruments in these areas. Our exclusivity rights in these four areas will be extended unless we fail to fulfill the minimum order placement requirements. We are currently seeking collaboration with distributors and developing markets for Xinhua instruments. Inventory has been purchased, imported, and is stocked at our corporate headquarters. A website was developed for business to consumer and business to business sales of Xinhua products. We have been pursuing marketing initiatives such as, advertising online through Google Adwords and other sites, as well as, through traditional methods like direct mail and sales calls. Additionally, we have been participating and responding to bid requests and requests for quotations from government, educational, and business organizations.

Acquisitions of Companies Complementary to the Company

Another major corporate focus is for the Company to acquire other profitable vaccine companies or vaccine production related companies, such as those producing materials for vaccine production, in China. Such an acquisition may help support our development of our in-house vaccine candidates by providing us with operating cash flows, lower cost for materials used in our vaccine production, a skilled work force pool in vaccine production, and distribution channels. We believe these companies will be complementary to us and make us more competitive.

On July 31, 2008, the Company completed the acquisition of Hohhot Xinheng Baide Biotechnology Co. Ltd., (“XHBD”), in which the Company purchased 51% of the outstanding capital interests of XHBD for RMB 6 million (approximately US$ 881,000). XHBD was incorporated on May 17, 2006 under the laws of the People’s Republic of China (“PRC”) as a limited company. XHBD is located in the city of Hohhot in Inner Mongolia, China. The primary operations of the Company are the manufacture and distribution of bovine serum products, which are used in research and production of vaccines. We completed the 51% acquisition of Xinheng Baide on July 31, 2008 and its operations are included in our consolidated financial statements beginning August 1, 2008. At July 1, 2009, XHBD changed its name to Bio-Bridge Xinheng Baide (Inner Mongolia) Biotechnology Co. Ltd. (“Bio-Bridge XBB”, “XBB”).

The demand for bovine serum in Chinese market is decreasing as more vaccine producers switch to production procedures using low-serum or serum-free cell culture systems. As such, the Company is currently under negotiation with a third party for the sale of its interest in XBB. At this stage of negotiation, it became evident that the recorded value of the goodwill to the XBB segment was impaired. The Company’s management recorded an impairment of goodwill at September 30, 2010 of $243,248.

Joint Venture

On June 9, 2009, Bio-Bridge Science (HK) Co., Ltd., a wholly-owned subsidiary of Bio-Bridge Science, Inc. entered into an equity joint venture contract with JR Scientific Inc., a California based manufacturer of classical and custom cell culture medium and sera products, and several other investors to form a new cell culture medium joint venture in Beijing, China. The Company invested RMB 5,100,000 (approximately US$732,000) in cash in the joint venture for 51% of the equity and JRS contributed certain technology for 15% of the equity. The balance of the equity was purchased by other investors, including 11% by China Diamond, an entity controlled by Trevor Roy, one of our directors.

On October 16, 2009, Bio-Bridge Science Inc. received a business license from the Beijing Administration for Industry and Commerce of the PRC indicating approval of the formation of Bio-Bridge JRS Biosciences (Beijing) Co., Ltd. (“Bio-Bridge JRS”). Bio-Bridge JRS was officially established at the end of October 2009.

The plant was fitted-out and major equipment has been purchased and installed. The fit-out has been completed and the facility is rated for all-year production, including conditions of extreme cold, heat, and humidity. The major production technology has been transferred from JRS to the JV technicians, and cell culture medium samples have been produced. The produced samples have been tested against those produced by our major competitors, and have performed very well. We expect that Bio-Bridge JRS will begin to formally produce and sell cell culture medium and related products at the fourth quarter of 2010. Major marketing activities are planned for first quarter 2011.

Results of Operation

Three-Month Period Ended September 30, 2010 and September 30, 2009

For the three months ended September 30, 2010 and 2009, total sales were $102,852 and $142,901, and the cost of goods sold were $57,810 and $92,052, or 56% and 64% of sales, respectively. Sales of Xinhua surgical instruments were $27,118 and $19,405 respectively for the three months ended September 30, 2010 and 2009, and the cost of goods sold were $13,195 and $9,541, or 49% of sales for both periods. The decrease in total sales is the result of the decrease in sales of bovine serum in Bio-Bridge XBB. The demand for bovine serum in Chinese market is decreasing as more vaccine producers switch to production procedures using low-serum or serum-free cell culture systems. The increase in sales of Xinhua surgical instruments is the result of our increasing efforts to acquire larger customers.

For the three months ended September 30, 2010 and 2009, research and development expenses were $38,898 and $69,308, respectively. The decrease of $30,410 in research and development expenses is due to the decrease in purchase of research materials during the three months ended September 30, 2010.

For the three months ended September 30, 2010 and 2009, general and administrative expenses were $308,589 and $308,704, respectively.

For the three months ended September 30, 2010 and 2009, selling and distribution expenses were $29,094 and $57,619, respectively. The decrease of $28,525 is primarily due to the decrease in the sales activities of Bio-Bridge XBB.

For the three months ended September 30, 2010 and 2009, interest expenses were $2,226 and $340, respectively. The increase of $1,886 is primarily due to fluctuations in the exchange rate of US Dollar to Chinese RMB in our subsidiaries in China.

For the three months ended September 30, 2010, impairment of goodwill was $243,248, compared to $0 for the three months ended September 30, 2009. The impairment was resulted from the deterioration in the market for XBB’s bovine serum, based on management’s assessment as of September 30. 2010.

Net loss for the three months ended September 30, 2010 and 2009 were $566,261 and $1,315,679, respectively. The decrease of $749,418 in net loss is mostly the combination effect of the change in derivative liability fair value, which was $10,752 gain for the three months ended September 30, 2010, compared to $958,147 loss for the three months ended September 30, 2009, and the impairment of goodwill, which was $243,248 for the three months ended September 30, 2010, compared to $0 for the three months ended September 30, 2009.

Nine-Month Period Ended September 30, 2010 and September 30, 2009

For the nine months ended September 30, 2010 and 2009, total sales were $310,693 and $582,925, and the cost of goods sold were $203,952 and $376,780, or 66% and 65% of sales, respectively. Sales of Xinhua surgical instruments were $76,024 and $54,512 respectively for the nine months ended September 30, 2010 and 2009, and the cost of goods sold were $37,280 and $23,354, or 49% and 43% or sales, respectively. The decrease in total sales is the result of the decrease in sales of bovine serum in Bio-Bridge XBB. The demand for bovine serum in Chinese market is decreasing as more vaccine producers switch to production procedures using low-serum or serum-free cell culture systems. The increase in sales of Xinhua surgical instruments is the result of our increasing efforts to acquire larger customers.

For the nine months ended September 30, 2010 and 2009, research and development expenses were $171,764 and $148,960, respectively. The increase of $22,804 is due to the increase in purchase of research materials in 2010.

For the nine months ended September 30, 2010 and 2009, general and administrative expenses were $2,647,960 and $808,109, respectively. The increase of $1,839,851 is mainly due to the compensation cost for issuing common stock warrants to two directors, which was $1,521,805, an increase in depreciation expense after putting our laboratory facility into service in mid-2009, and the increase in expenses of vested stock options.

For the nine months ended September 30, 2010 and 2009, selling and distribution expenses were $97,498 and $148,581, respectively. The decrease of $51,083 is primarily due to the decrease in the sales activities of Bio-Bridge XBB.

For the nine months ended September 30, 2010 and 2009, interest expenses were $5,294 and $637, respectively. The increase of $4,657 is primarily due to fluctuations in the exchange rate of US Dollar to Chinese RMB in our subsidiaries in China.

For the nine months ended September 30, 2010, impairment of goodwill was $243,248, compared to $0 for the nine months ended September 30, 2009. The impairment was resulted from the deterioration in the market for XBB’s bovine serum, based on management’s assessment as of September 30. 2010.

Net loss for the nine months ended September 30, 2010 and 2009 were $3,030,009 and $594,739, respectively. The increase of $2,435,270 in net loss is mostly the combination effect of the increase in general administrative expenses, the decrease in gain on derivative liability fair value, which was $15,665 for the three months ended September 30, 2010, compared to $268,271 for the three months ended September 30, 2009, and the impairment of goodwill, which was $243,248 for the nine months ended September 30, 2010, compared to $0 for the nine months ended September 30, 2009.

Liquidity and Capital Resources

Our principal sources of liquidity are cash and cash equivalent balances, which was $568,188 at September 30, 2010.

Net cash used in operating activities for the nine months ended September 30, 2010 and 2009 were was $968,051 and $983,069 respectively.

Net cash used in investing activities for the nine months ended September 30, 2010 and 2009 were was $357,751 and $527,883 respectively. The decrease is primarily due to the decrease in fixed assets purchases.

Net cash provided by financing activities for the nine months ended September 30, 2010 and 2009 were was $307,059 and $1,851,747 respectively. The decrease is primarily due to the decrease in the proceeds from issuance of common stock.

To date, our operations have been funded through issuances of our common stock and preferred stock whereby we raised an aggregate $8,365,888 from inception through September 30, 2010.

Critical Accounting Policies

Our discussion and analysis of our financial condition and results of operations are based on our consolidated financial statements, which have been prepared in accordance with accounting principles generally accepted in the U.S. The preparation of these financial statements requires us to make estimates and judgments that affect the reported amounts of assets, liabilities, revenues and expenses for each period. The following represents a summary of our critical accounting policies, defined as those policies that we believe are the most important to the portrayal of our financial condition and results of operations and that require management's most difficult, subjective or complex judgments, often as a result of the need to make estimates about the effects of matters that are inherently uncertain.

Use of Estimates

Revenue Recognition

Accounts Receivable

Stock-Based Compensation

The Company periodically issues stock options and warrants to employees and non-employees in non-capital raising transactions, for services, and for financing costs. The Company accounts for stock option and warrant grants issued and vesting to employees based on the authoritative guidance provided by the Financial Accounting Standards Board (“FASB”). The Company accounts for stock option and warrant grants issued and vesting to non-employees in accordance with the authoritative guidance of the FASB whereas the value of the stock compensation is based upon the measurement date as determined at either a) the date at which a performance commitment is reached, or b) at the date at which the necessary performance to earn the equity instruments is complete. Non-employee share-based compensation charges generally are amortized over the vesting period on a straight-line basis. In certain circumstances where there are no future performance requirements by the non-employee, option grants are immediately vested and the total share-based compensation charge is recorded in the period of the measurement date.

The fair value of Bio-Bridge’s common stock option grants are estimated using the Black-Scholes-Merton option pricing model, which uses certain assumptions related to risk-free interest rates, expected volatility, expected life of the common stock options, and future dividends. Compensation expense is recorded based upon the value derived from the Black-Scholes option pricing model, and based on actual experience. The assumptions used in the Black-Scholes-Merton option pricing model could materially affect compensation expense recorded in future periods.

Impairment of Long-Lived Assets, Goodwill and Intangible Assets

We review long-lived assets whenever events or changes in circumstances indicate the carrying amount of an asset may not be recoverable in accordance with the authoritative guidance provided by the FASB. Our long-lived assets, such as property and equipment, are reviewed for impairment when events and circumstances indicate that depreciable or amortizable long lived assets might be impaired and the undiscounted cash flows estimated to be generated by those assets are less than the carrying amount of those assets. When specific assets are determined to be unrecoverable, the cost basis of the asset is reduced to reflect the current value.

We use various assumptions in determining the current fair value of these assets, including future expected cash flows and discount rates, as well as other fair value measurements. Our impairment loss calculations require us to apply judgment in estimating future cash flows, including forecasting useful lives of the assets and selecting the discount rate that reflects the risk inherent in future cash flows. If actual results are not consistent with our assumptions and judgments used in estimating future cash flows and asset fair values, we may be exposed to future impairment losses that could be material to our results.

Inventory Valuation

Inventories are stated at the lower of cost or market. Market is defined as current replacement cost, except that market should not exceed the net realizable value and should not be less than net realizable value reduced by an allowance for an approximately normal profit margin. The cost of inventories is determined by using the first-in, first-out method. We perform a monthly analysis of our inventory balances to determine if the carrying amount of inventories exceeds their net realizable value. Our determination of estimated net realizable value is based on customer orders, market trends and historical pricing. If the carrying amount exceeds the estimated net realizable value, the carrying amount is reduced to the estimated net realizable value.

Derivative Financial Instruments

The Company evaluates all of its financial instruments to determine if such instruments are derivatives or contain features that qualify as embedded derivatives. For derivative financial instruments that are accounted for as liabilities, the derivative instrument is initially recorded at its fair value and is then re-valued at each reporting date, with changes in the fair value reported in the condensed consolidated statements of operations. For stock-based derivative financial instruments, the Company uses both the Black-Scholes-Merton option pricing models to value the derivative instruments at inception and on subsequent valuation dates. The classification of derivative instruments, including whether such instruments should be recorded as liabilities or as equity, is evaluated at the end of each reporting period. The Company does not use derivative instruments to hedge exposures to cash flow, market or foreign currency risks.

Recent Accounting Pronouncements

In April 2010, the Financial Accounting Standard Board (FASB) issued new accounting guidance to clarify that an employee share-based payment award with an exercise price denominated in the currency of a market in which a substantial portion of the entity's equity securities trades should not be considered to contain a condition that is not a market, performance, or service condition. Therefore, an entity would not classify such an award as a liability if it otherwise qualifies as equity. The amendments are effective for fiscal years, and interim periods within those fiscal years, beginning on or after December 15, 2010. The Company does not expect adoption of this standard will have a material on its consolidated financial position or results of operations.

Commitments

Royalty and License Arrangements

Liang Qiao, M.D., our co-founder and chief executive officer, is one of the two co-inventors of our core technology that was assigned to Loyola University Chicago in April 2001. Under an agreement with Loyola University Chicago, we have obtained exclusive rights to this technology for use in its future products within the United States, Japan and the People's Republic of China, including mainland China, Hong Kong, Taiwan and Macau. The license continues perpetually or for the maximum period of time permitted by law, unless terminated earlier under the terms of the agreement. Pursuant to this agreement, Loyola receives a royalty of 4% from the net profit for all uses of the licensed technology, including uses under sublicenses. As of September 30, 2010, we had not generated any revenues from the sale of any products under development, nor had we received any revenues from sublicenses.

Item 3. Quantitative and Qualitative Disclosure about Market Risk

The Company is a smaller reporting company and is not required to provide the information required by this.

Item 4. Controls and Procedures

(a) Evaluation of disclosure controls and procedures. As of the end of the period covered by this report, we carried out an evaluation, under the supervision and with the participation of our management, including our Principal Executive Officer and Principal Financial Officer, of the effectiveness of the design and operation of our disclosure controls and procedures, as defined in Rules 13a-15(e) and 15d-15(e) under the Securities Exchange Act of 1934, as amended. Based upon that evaluation, our Principal Executive Officer and Principal Financial Officer concluded that our disclosure controls and procedures were effective as of the end of the applicable period to ensure that the information required to be disclosed by us in reports that we file or submit under the Exchange Act (i) is recorded, processed, summarized and reported within the time periods specified in Securities and Exchange Commission rules and forms and (ii) is accumulated and communicated to our management, including our Principal Executive Officer and Principal Financial Officer, as appropriate to allow timely decisions regarding required disclosures.

(b) Changes in internal controls over financial reporting. There was no change in our internal control over financial reporting during our most recent fiscal quarter that has materially affected, or is reasonably likely to materially affect, our internal control over financial reporting.

PART II - OTHER INFORMATION

Item 1. Legal Proceedings

Not Applicable.

Item 1A. Risk Factors

There have been no material changes in the risk factors previously disclosed in Form 10-K we filed with the SEC on March 31, 2010.

Item 2. Unregistered Sales of Equity Securities and Use of Proceeds

Not applicable.

Item 3. Defaults Upon Senior Securities

Not applicable.

Item 4. Submission of Matters to a Vote of Security Holders

Not applicable.

Item 5. Other Information

Not applicable.

Item 6. Exhibits

The exhibits listed in the Exhibit Index are filed as part of this report.

SIGNATURES

In accordance with Section 13 or 15(d) of the Exchange Act, the registrant caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.

Bio-Bridge Science, Inc.

Date: November 15, 2010

/s/ Dr. Liang Qiao

By: Dr. Liang Qiao

Chief Executive Officer

(Principal Executive Officer)

EXHIBIT INDEX

3.1(i)*		Certificate of incorporation of the registrant, as currently in effect

3.1(ii)*		Bylaws of the registrant, as currently in effect

3.1(iii)**		Certificate of Designation of Series A Preferred Stock

31.1		Certification of Principal Executive Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002

31.2		Certification of Principal Financial Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002

32		Certifications of Principal Executive Officer and Principal Financial Officer pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of Sarbanes-Oxley Act of 2002

* Previously filed with the Securities and Exchange Commission pursuant to Registration Statement No. 333-121786.

** Previously filed as an exhibit to the Registrant's Form 10-KSB for its year ended December 31, 2006.

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BGES Bio Bridge Science Inc (CE)