Dear Colleague,
The fundamental key to financial success for pharmaceutical and biotech companies lies in their ability to bring safe and effective drugs and devices to the market place. Clinical trials are an essential step in this process. Completing them successfully is an expensive and time consuming process, which must be achieved with as much precision, precaution and cost-effectiveness as possible.
Keeping abreast of the latest developments and understanding how they fit together to improve overall trial practice is vital. With e-clinical trials, adaptive strategies, the application of genomics and exciting new trial locations, the possibilities for innovation are endless. By attending this conference you will keep abreast of these developments and understand how they can interact with each other to produce trials that will give your business the competitive edge required in today’s market place.
Clinical Trials 2008 will bring to together leading professionals in the field of clinical operations and development, providing the ideal networking and information exchange platform for clinical executives from pharmaceutical companies, contract research organizations, and regulatory associations.
Why should you attend?
This Conference will bring together market leaders, specialists and renowned academics to:
Discuss new methods of data capture, the potential it offers for large scale trials and how to avoid the pitfalls associated with selecting and implementing such an e-clinical system.
Discover what are the benefits of the latest adaptive trial strategies, and how can the difficulties in implementation be overcome? What are the expert recommendations for integrating new technologies into existing business practice?
Understand how do local regulatory guidelines and systemic requirements interrelate?
Explore innovative strategies for outsourcing, what you should be looking for in a CRO? What considerations are involved in writing and managing a sensible contract? How can you take advantage of the global market for clinical trials?
Develop strategies for patient recruitment and retention
Who Will Attend:
From pharmaceutical, biotech and CROs:
Directors and Heads of:
Clinical Research and Development
Clinical Research Services
Clinical Operations
Clinical Data Management
Clinical IT
Clinical Trials
Medical Affairs
Regulatory Affairs
Compliance
Quality Control/Assurance/
Clinical Study Design
Safety Surveillance
Subject Recruitment
e-Clinical Systems
Key Speakers :-
Dr Dave Moskowitz, CEO, Genomed
Fiona Glenny, Project Lead, EDC Track, e-Clinical, Lundbeck
Dr Thomas Bethke, Medical Director, Germany, Nycomed
Zoe Garrett, Analyst, Centre for Health Technology Evaluation, NICE
Tom Parke, Head of Clinical Trials Solutions, Tessella
Richard Young, Director of Business Development, CMED Clinical Research Services
Carmen Salazar, Senior Clinical Pharmacist, Genzyme
Francis P. Crawley, Executive Director, Good Clinical Practice Alliance – Europe
Vinka Ljubimir, Clinical Study and Data Management, Pfizer
John Shillingford, Head of Global Clinical Operations, Averion International (formerly Hesperion)
Dr Norbert Benda, Statistical Methodology, Novartis Pharma
Dr Michael Herschel, Director, Clinical Research, GlaxoSmithKline
Dr Göran Gannedahl, President, NMCT
For more information kindly visit: http://www.bharatbook.com/
