Research and Markets: Clinical Data Management 2010 Summit - 19 October, 2010, ITC Maratha, Mumbai, India - Register Now
22 September 2010 - 1:49PM
Business Wire
Research and Markets
(http://www.researchandmarkets.com/research/e1c7a6/clincal_data_manag)
has announced the addition of the "Clinical Data Management 2010"
conference to their offering.
19, October 2010, ITC Maratha, Mumbai, India "Creating an
optimised data integration & standardised data collection for a
secured future for CDM"
The pharmaceutical business is under huge pressure and needs to
be more competitive if it is going to stay successful. Every day
companies generate large amounts of data, much of which is never
fully leveraged. Traditional approaches to data collection and
management prevent the full curation of all data within a company,
leading to a substantial opportunity lost for that company. Why is
this? Do companies really understand the full power of the data
they own? What can be done by your members of your organisation to
advance the thinking and technology?
India has developed into a super power for IT skills and has
become a major hub for pharmaceutical and biotech manufacturing and
contract research, the outsourcing business in various other
segments is also exhibiting promise. Clinical trial data management
and statistical analysis is one such area which is growing rapidly,
accompanied by a variety of players entering into different models
of this business. This conference will reflect on the data
management business in India and review the emerging outsourcing
models in this growing pharma industry.
Few tasks in R&D rival the complexity of clinical data
management while its importance in providing clean and correctly
mapped data carries direct impact on the success of drug
submission. In times of increasing trial costs and the rising
threat of clinical outsourcing, keeping ahead of competition and
abreast of the latest developments is paramount to surviving a
harsh CDM climate. The role of data managers has experienced a
fundamental shift from doer to controller, from data collector to
system administrator. This year's conference will capture the
essence of electronic data integration, interface interoperability
and system optimisation to spearhead a global understanding of data
standardisation and usher clinical data management into a time- and
cost-efficient second generation. Meticulous care has been taken to
offer practical solutions and real-life case studies to combat the
challenges of CDM. Market leaders will share their ideas and
outline their action plan to crucially assist your decision-making
process when improving Data capture and integration, Outsourcing
strategies, Data cleaning, validation and mapping, CDISC
implementation and compliance, Vendor and project management
skills
CDM 2010 will provide you with the data that you need to
recognize this complex and rapidly-expanding sector. Knowing the
future market, and what impact will that have on future business
opportunities? This is your opportunity to stay ahead by learning
the latest trends and networking with the trend setters.
It gives us immense pleasure in welcoming you to the Clinical
Data Management '2010
Key themes discussed at this Summit:
- Current trends of clinical data management & how can you
take advantage of the current global market
- Driving for success is highly vital, but are you driving as
smart as with strategies and tips on the most efficient ways to
register clinical trials and results while best utilizing available
resources
- Data management, CMC SCM, operational requirements & CRO
infrastructure in India & South Asia
- Discovering cutting edge EDC technology and assessing the
latest database and data capture systems available
- Leverage the importance of CDISC compliance and standardized
data capture to achieve effortless submission
- Overview of the various types of data that data managers
working in oncology handle and the associated challenges
- How to land up in finding the right BPO partner
- Achieving consistent application & implementation of data
standards to speed trial process
- Identifying the key critical factors for developing knowledge
and skills in vendor management
- Attain solid vendor management skills to expertly juggle
outsourced tasks
- Discovering technologies and strategies for successful clinical
data management
- Avoiding potential pitfalls of data management
- Working with limited budget to ensure on time study
completion
- Be prepared for audits; site, CRO and in-process trial
audits
Key Topics Covered:
08:30 Coffee and registration
09:30 Chair's opening remarks
Zinobia Madan, Founder & Managing Director, ClinOma
Healthcare
9:40 Examining the current status and future prospects of
bioinformatics & data management in India
10:20 Driving Data Management the Cost, Future and Unknown
11:00 Morning coffee & Discussion
11:20 Selecting the optimal EDC provider to receive quality
data
Dinesh Pillaipakkamnatt, Global Head - DB Programming, IIS TS,
Norvartis
12:00 Panel Discussion: Evaluating key emerging markets for
improved strategy
Moderator
Panelists Anil Arekar, Senior Consultant Biostatistics - Asia
Pacific, Johnson & Johnson Deepti Sanghavi, Medical Advisor-
Clinical Research, Wockhardt Poonam Sule, Senior Clinical Study
Manager, Pfeizer
12:40 - Networking Luncheon - Take your discussions further
& build new relationships in a relaxed & informal
setting
13:30 Trial Design Considerations
Anil Arekar, Senior Consultant Biostatistics - Asia Pacific,
Johnson & Johnson
14:10 Impact of advanced technology in today's clinical
world
14:50 'Clinical Operations and Data Management - Together we
deliver a Good Quality Trial Faster'.
Chirag Trivedi, Head - Medical Affairs Clinical Operations,
Sanofi Aventis
15:20 Afternoon tea
15:40 Panel Discussion: Overcoming regulatory challenges in
Asian clinical data management - Now and Future
Moderator Milind Antani, Head-Pharma LifeSciences group, Nishith
Desai Associates
Panelists Milind Sardesai, Medical & Regulatory Affairs,
Clinical Research Physician, Chiltern
16:20 Managing external vendors from a sponsor perspective
17:00 Pharmaceutical Programming: From CRFs to Tables, Listings
and Graphs, a process overview with real world examples
17:00 Pharmaceutical Programming: From CRFs to Tables, Listings
and Graphs, a process overview with real world examples
Jino Joseph, Senior SAS Programmer, GlaxoSmithKline
17:30 - Chairperson's closing remarks and end of conference
Zinobia Madan, Founder & Managing Director, ClinOma
Healthcare
17:40 - Networking Drinks - Take your discussions further &
build new relationships in a relaxed & informal setting.
Speakers:
- Dinesh Pillaipakkamnatt, Global Head - DB Programming, IIS TS,
Norvartis
- Celestine Juliet, Project Manager, Regulatory Affairs, Clinical
Research, Cipla
- Chirag Trivedi, Head - Medical Affairs Clinical Operations,
Sanofi Aventis
- Poonam Sule, Senior Clinical Study Manager, Pfeizer
- Anil Arekar, Senior Consultant, Biostatistics - Asia Pacific,
Johnson & Johnson
- Deepti Sanghavi, Medical Advisor - Clinical Research,
Wockhardt
- Milind Antani, Head-Pharma LifeSciences group, Nishith Desai
Associates
- Zinobia Madan, Founder & Managing Director, ClinOma
Healthcare
- Milind Sardesai, Medical & Regulatory Affairs, Clinical
Research Physician, Chiltern
- Jino Joseph, Senior SAS Programmer, GlaxoSmithKline
For more information visit
http://www.researchandmarkets.com/research/e1c7a6/clincal_data_manag