Event on 2012-07-05 08:30:00
Key Themes Discussed at this Summit:
• Where does India stand in the current global clinical trials market and how to take advantage of the same? How can you take advantage of the global market for clinical trials?
• Discovering technologies and strategies for successful clinical trial management
• Strategies in conducting successful interventional oncology trials in India
• Setting up clinical trial research hub & techniques for applying risk management principles.
• Discovering global opportunities in clinical trial and selecting the right partners to penetrate successfully into the Indian market
• Identifying ideal clinical sites and strategizing patient recruitment and clinical sites management in India to develop appropriate clinical studies
• Avoiding potential pitfalls of trials agreement
• Regulatory review at the Drugs Controller General of India (DCGI) and Central
Drugs Standard Control Organization (CDSCO): science, quality, and speed
• Effectively incorporating GCP & GCPs – Knowing what TO-DO and what NOT TO-DO
• Effectively managing cold chain and logistics in clinical trials
• Optimising clinical trials operation effectiveness and ROI through strategic site,patient, data and risk management in the regulated markets
• What are the issues with off-shoring trials to countries such as India & South Asia? – Solutions?
• Motivating and managing clinical project teams to improve timeline and progress
• Exploring the efficacy and safety of new interventions in clinical trials
• Drawing and retaining clinical talent pool to minimise turnover in clinical studies
• Next generation of clinical trials – How big will the market be?
Key Speakers :
• Arun Bhatt, President, Clininvent Research
• Bhaswat S. Chakraborty, Senior Vice President, Research and Development, Cadila
• Girish S. Gudi, Vice President, Drug Metabolism and Pharmacokinetics, Glenmark Pharmaceuticals
• Ammar Raza, Associate Director- Medical Affairs, AstraZeneca
• Viraj Rajadhyaksha, Associate Director - Medical Liaison, Sanofi-Aventis
• Arani Chatterjee, Vice President, Clinical Research, Panacea Biotec
• Rohit Arora, Deputy Director, Sanofi Pasteur
• Prashant Bodhe, Head Regulatory Affairs & Vice President Operations, DMRI
• Subashri Shivkumar, Hub Unit Director-Regional Clinical Operations, Bristol-Myers Squibb
• Chirag Trivedi, Head - Medical Affaris Clinical Operations, Sanofi-Aventis
• Milind Antani, Head-Pharma LifeSciences group, Nishith Desai Associates
• Farzana Lakdavala, Medical Advisor, Project Manager Clinical Research, Wockhardt
• Murtuza S. Bughediwala, General Manager, Clinical Operations & Business Development, Clininvent Research
• Poonam Sule, Senior Manager - Clinical Research (International), Wockhardt
• Ashish Gawde, Senior Manager- Clinical Research, BAYER
• Jeroze Dalal, General Manager Clinical Operations, GlaxoSmithKline
Plus many more
Who Should Attend:
Vice Presidents, Directors Heads & Managers of:
• Clinical Research & Development
• Clinical Research Services
• Clinical Operations
• Clinical Data Management
• Clinical IT
• Clinical Trials
• Medical Affairs
• Regulatory Affairs
• Compliance
• Quality control / Assurance/GCP
• Clinical Study Design
• Safety Surveillance
• Subject Recruitment
• E-Clinical Systems
Target Audience – Industry:
• Pharmaceutical Organisations
• Generic pharmaceutical companies
• Contract Research Organisations
• Patient Recruitment Companies
• Government- Department of Health
• Non-profit organisations/ Association
• Academics
• Consultants
Why Should You Attend?
Get more from the event, with a broader scope bringing the whole communications value chain together. Enjoy and make the best out of our dedicated networking drinks time, meet the leading international vendors showcasing the products of tomorrow in the co-located exhibition. Expand your knowledge of the latest business models and strategies in the high-level conference.
Ordering Delegate Pass – Register Now
Ordering is simple! You can simply email or call and book your seats on
TEL: +91 (44) 23770517 . Email – delegate@virtueinsight.com
For this one day conference, conference fee is 05,000 INR + tax per person
Should you have any queries, please feel free to write to us pradeep@virtueinsight.com, pradeepvic@yahoo.com
at ITC Maratha- The Luxury Collection
Sahar, India
The 2012 Positive Youth Development Institute
Event on 2012-07-23 08:00:00
Continuing Education Credits are available for this event:
1.5 general CEUs
Conference Agenda
Special rates at area lodging:
The Black Bear Inn Days Inn Hotel
4 Godfrey Drive 250 Odlin Rd.
Orono, Maine Bangor, Maine
.95 + tax .00 + tax
207-866-7120 207-942-8272
Reserve by July 8th
Keynote Speakers
Jeffrey A. Butts (Ph.D., University of Michigan) is director of the Research and Evaluation Center at John Jay College of Criminal Justice, City University of New York (CUNY), and senior research advisor at the Vera Institute of Justice in New York City. His work focuses on research and evaluation projects designed to discover and improve policies and programs for at-risk and disconnected youth, especially those involved with the justice system. He has more than 25 years of experience in research, program evaluation, policy analysis, and direct services. Dr. Butts has published two books, dozens of reports for the U.S. Department of Justice and other agencies, and articles in journals such as the American Journal of Criminal Law, Crime and Delinquency, Criminal Justice Policy Review, Judicature, Law & Policy, Juvenile & Family Court Journal, and Youth & Society. His research findings and policy views have been covered by the New York Times, the Washington Post, the Los Angeles Times, the Chicago Tribune, the San Francisco Chronicle, the Miami Herald, the Economist, Christian Science Monitor, BusinessWeek, US News & World Report, Time Magazine, National Public Radio, and CNN, among others. Previously, Jeff was a Research Fellow with Chapin Hall at the University of Chicago, director of the Program on Youth Justice at the Urban Institute in Washington, DC, and a senior research associate with the National Center for Juvenile Justice. A native of Springfield, Ohio, Jeff began his career as a drug and alcohol counselor with the juvenile court in Eugene, Oregon.
Gil G. Noam is the Founder and Director of the Program in Education, Afterschool & Resiliency (PEAR) and an Associate Professor at Harvard Medical School and McLean Hospital. Trained as a clinical and developmental psychologist and psychoanalyst in both Europe and the United States, Dr. Noam has a strong interest in supporting resilience in youth, especially in educational settings. He served as the director of the Risk and Prevention program, and is the founder of the RALLY Prevention Program, a Boston-based intervention that bridges social and academic support in school, afterschool, and community settings. Dr. Noam has also followed a large group of high-risk children i 
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