8th Annual Clinical Trials Summit will bring together leaders from across pharma, biotech and academia to share case studies and best practices on effective clinical trial management and vendor oversight.
Event Date : May24, 2017.
Location : Mumbai, India
Virtue Insight's 8th Annual Clinical Trials Summit will bring together leaders from across pharma, biotech and academia to share case studies and best practices on effective clinical trial management and vendor oversight. The 2017 program focuses on key issues and opportunities in the clinical trial industry, including Patient Recruitment, Site Selection, Data Integration, Existing Data Sources, Mobile Tech, Project Management, Outsourcing, Vendor Management, Risk-Based Monitoring, Clinical Auditing, Regulatory Authorities, pharmaceutical industries, contract research organizations, patient associations, and academic groups are represented. This conference is known to facilitate the interaction between all stakeholders, speakers and participants, thus encouraging lively Q&A sessions without cultural barriers. In addition, as usual, this Conference represents a great opportunity to network with all players involved in drug and device development.
Virtue Insight also offers comprehensive sponsorship packages, which includes presentation opportunities, exhibit space, branding and networking with specific prospects.
KEY THEMES DISCUSSED:-
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
DATA - Collection, Design, Storage, Execute and Manage clinical trials - an architect's perspective
Updates on development for safety reporting in Indian clinical trial regulation
Be part of a major networking opportunity
K. BANGARURAJAN, Deputy Drugs Controller (India), CDSCO
RAJENDRA H. JANI, Advisor/ Independent Subject Expert, Zydus Cadila
ARUN BHATT Consultant - Clinical Research & Development
VIVEK GUPTA, Worldwide VP, Acceliant
MANMOHAN SINGH APAC Regional Medical Director Pfizer
YASMIN SHENOY, Director-Regulatory Affairs, Sanofi-aventis
SRIRUPA DAS, Associate Director-Medical Affairs, Abbott
JYOTSNA PATWARDHAN, Head Development QA, Novartis
ABHAY PHANSALKAR, Head Clinical Trials, Cipla
WHO SHOULD ATTEND:-
CEOs, CTOs, CIOs, 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.
For More Information -
JSB Conference Events team
Mobile: +91 9987295242