8th Annual Clinical Trials Summit

8th Annual Clinical Trials Summit is organized by Virtue Insight and would be held on May 24, 2017 at Kohinoor Continental Hotel, Mumbai, Maharashtra, India.

KEY THEMES DISCUSSED :
• Key drivers behind achieving a successful and sustainable clinical trails strategy in 2017
• Develop faster, more effective strategies by setting up big data with the power of sophisticated analytics
• Outsourcing early stage manufacturing
• Benefits and challenges with using local and international vendors
• Develop trial design and elaborate patient access
• Span all phases of clinical and observational research
• How we use mobile in clinical trials nowadays? What is the present barrier?
• Integrated approaches to using digital as a clinical Tool: Real world trials and population health in the east India
• The Impact of in-life unjust information on clinical trials execution
• Observing operational progress and efficiency of a study or an asset in critical for drug development success
• Strategic partnerships between Sponsor-CRO and how the industry has evolved in the past 5 years

KEY SPEAKERS :
• MANMOHAN SINGH, APAC Regional Medical Director, Pfizer
• RAJENDRA H. JANI, Advisor/ Independent Subject Expert, Zydus Cadila
• SUMIT MUNJAL, Medical Director Lead, Global Medical Safety, Head of Mature Established products, Takeda Pharmaceuticals (UK)
• YASMIN SHENOY, Director-Regulatory Affairs, Sanofi-aventis
• SRIRUPA DAS, Associate Director-Medical Affairs, Abbott
• CHIRAG TRIVEDI, Director & Head of Clinical Study Unit, Sanofi-aventis
• TAPANKUMAR M. SHAH, Country Head-Site Management & Monitoring, AstraZeneca
• MUKESH KUMAR, Global Head-Clinical Management, Dr. Reddy's Laboratories
• SHILPA RAUT, Regional Training Head-Asia, Middle East and Africa Cluster, Novartis
• NARESH TONDARE, Head-India and Nepal Regulatory Affairs, Glenmark Pharmaceuticals
• MILIND ANTANI, Partner In-Charge-Pharma LifeSciences, Nishith Desai Associates
• JYOTSNA PATWARDHAN, Head Development QA, Novartis
• ABHAY PHANSALKAR, Head Clinical Trials, Cipla
• PRAVIN GHADGE, Head-Medical Writing & Pharmacovigilance, Reliance Life Sciences Plus Many More..

WHO SHOULD ATTEND :
CEO's, CTO's, CIO's, Presidents, 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.

• Early Bird Discounted Price– 1 Delegate Pass - (INR 6,000 + Tax (15%) per delegate) (Ends 10th April 2017 )
• Standard Price– 1 or 2 Delegates - (INR 8,000 + Tax (15%) per delegate) (From 11th April 2017)
• Group Discounts – 3 or 4 Delegates - (INR 7,000 + Tax (15%) per delegate)
• Group Discounts – 5 and above Delegates - (INR 6,000 + Tax (15%) per delegate)
• Conference Sponsor & Exhibition Stalls are also available.

REGISTRATION PROCESS :
In order to register simply fill in the last page of the attached file and email is back to me or you can simply email me your invoice details in the below mentioned format.

Company Name & Address :
We also have sponsorship opportunities available for the event which gives you an opportunity to speak/exhibit and create brand awareness. In addition, the networking opportunities in focused and relevant industry gathering provide the personal contact necessary for business development efforts. So kindly let me know if you would be interested in sponsorship packages for speaking opportunity or exhibiting at the conference.