FALLS CHURCH, Va., March 27, 2020 /PRNewswire-PRWeb/ -- Drug GMP Report
An FDAnews Newsletter
Inspection hotspots… certification… procedures… electronic data requirements… evolving trends in drug GMP enforcement…
Want access to the inner workings of the FDA or a trusted friend there to share insights into the interpretation and enforcement of cGMPs?
Turn to us today! Drug GMP Report is prepared with subscribers in mind. Its main goal is to support one in maintaining a competitive edge. This newsletter has the insights and latest information one must know to ensure processes, procedures and controls are compliant.
Each issue of Drug GMP Report will bring subscribers the latest news on:
•FDA inspections and warning letters, such as the agency's continuing focus on failures to document quality unit responsibilities
•Areas of increasing FDA oversight including cybersecurity and data integrity
•New traceability requirements as the FDA implements the landmark Drug Supply Chain Security Act
•FDA's quality-related policy guidance
•International quality trends, including joint recognition of GMP inspections
For the past 20 years, manufacturers have relied on Drug GMP Report for the latest on the FDA's interpretation and enforcement of cGMPS.
Bonus! Subscribers also receive critical documents within each issue, such as draft or final guidances, 483s and warning letters, proposed rules, the full text of proposed legislation and more.
Subscribe now to start a one-year subscription (12 issues) to Drug GMP Report for only $1,045. Take advantage of our 100% Money-Back Guarantee, we're confident the value one gains from Drug GMP Report will pay for itself many times over.
Drug GMP Report
An FDAnews Newsletter
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FDAnews is the premier provider of domestic and international regulatory, legislative, and business news and information for executives in industries regulated by the US FDA and the European Medicines Agency. Pharmaceutical and medical device professionals rely on FDAnews' print and electronic newsletters, books and conferences to stay in compliance with international standards and the FDA's complex and ever-changing regulations