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5th Annual Clinical Trials Summit 2014

5th Annual Clinical Trials Summit 2014 "A critical guide for successfully conducting clinical trials” 10th & 11th June 2014, Kohinoor Continental Hotel, Mumbai, India

 
PRLog - May 8, 2014 - MUMBAI, India -- 5th Annual Clinical Trials Summit 2014

"A critical guide for successfully conducting clinical trials”

10th & 11th June 2014, Kohinoor Continental Hotel, Mumbai, India

Day 1 (10th June)  – Workshop

Workshop Title - Clinical Trials in India in 2020

Analysing the US/EU Landscape in 2014 and find out on how customers in India can relate to what is happening elsewhere
How can Indian market benefit from this
The Indian Regulatory Environment – Including Vision for Indian R&D Community
Updates on Protocol Design / Complexity
Risk-based Monitoring
Clinical Trial Supply Chain Optimization
Transforming Indian R&D in 2014

Workshop Leader from Medidata (UK)

Day 2 (11th June)  – Conference

Key Themes Discussed at this Summit:

Overview of Indian healthcare and clinical trial system towards 2015
Analysing the recent government rules and guidelines
Discovering the new trends in global clinical trials and their role in India
Technologies that drive efficiencies in global clinical trials
Strategies to conduct successful interventional oncology trials in India
Updates on design of clinical drug
What are the expectations of regulatory authorities and what type of regulatory structure does India currently have?
Overcoming challenges faced in regulatory approval processes – obtaining drug/ clinical supplies import and export licenses in Asia
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
Adapting to India’s transformed regulatory landscapes to conduct clinical trials
Re-Thinking patient recruitment and patient experience
Finding the ideal partner in outsourcing your logistics operations in India how to identify smart packaging solutions to balance quality and costs
Identifying the decision criteria for partnering with the right vendors in Asia
How to manage risks in clinical trials effectively and how to successfully incorporate risk sharing models in clinical trials
Finding the right clinical trial supply chain model to optimize the costs
Avoiding mistakes in data collection and ensuring profitability and to understand the long term operation strategies for managing clinical trials.
Understanding new e-clinical technologies to improve data quality and optimise clinical outcomes
Next generation of clinical trials – How big will the market be?

Key Speakers:

Arun Bhatt, President, Clininvent Research
Bhavesh Kotak, Vice President, Astrazeneca
Sofi Joseph, Head – Regulatory Operations, Pfizer
Bhaswat Chakraborty, Senior VP & Chair, Research & Development Core Committee, Cadila Pharmaceuticals
Chirag Trivedi, Associate Director - Project Management & Strategic Initiatives, Sanofi
Ravisekhar Kasibhatta, Vice President – Clinical Research, Lupin
Kedar Suvarnapathaki, Head - Regulatory Affairs, Boehringer Ingelheim
Mubarak Naqvi, Senior Director & Head, Clinical Study Unit, Sanofi
Suresh Maroli, Head Clinical Pharmacology, Reliance Life Sciences
Ashwani Pandita, Head Quality Management & Training, Glenmark
Saji Vijayan, Head – Clinical Endpoint & Manager-Clinical Trials, Lupin
Sujay Salvi, Head, CTSM, SIRO Clinpharm
Prashant Bodhe, Associate Director, Quintiles Research
Deepti Sanghavi, Senior Medical Writer-Medical Writing, SIRO Clinpharm
Amey Mane, DGM-Medical Affairs, Wockhardt

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.

Target Audience-Industry:-

Pharmaceutical organisations
Generic pharmaceutical companies
Contract research organisations
Patient recruitment companies
Government - Department of health
Non-profit organisations/ Association
Consultants

Why Should You Attend:

5th Annual Clinical Trials Summit 2014 -“A critical guide for successfully conducting clinical trials” 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 expand your knowledge of the latest business models and strategies in the high-level conference. Show casing the products of tomorrow in the co-located exhibition.

Conference Booking Details:

Standard Price After Early Bird Discounted Time -
Conference Delegate Pass & Workshop - 1 or 2 Delegates (INR 7,000 + Tax (12.36%) per delegate)
Conference Only – 1 Day (INR 6,000 + Tax (12.36%) per delegate)

You can simply email or call and book your conference delegate seats on TEL: +917401150416. Email – nisha@virtueinsight.net

Group Discounts -
Conference Delegate Pass & Workshop - 3 and above Delegates - (INR 6,000 + Tax (12.36%) per delegate)
Conference Only – 1 Day (INR 5,000 + Tax (12.36%) per delegate)

You can simply email or call and book your conference delegate seats on TEL: +917401150416. Email – nisha@virtueinsight.net

Spot Registration on the day of the Conference - 2 Day Conference & Workshop - (INR 8,000 + Tax (12.36%) per delegate)

Conference Sponsor & Exhibition Stall - Should you wish to Sponsor, or purchase a Exhibition Stall (Booth) or a paid Speaker Slot, you can simply email your interest and queries to –TEL: +91 7401150416. Email – nisha@virtueinsight.net

Contact
Nisha
+917401150416
nisha@virtueinsight.net

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Source:Virtue Insight
City/Town:Mumbai - Maharashtra - India
Industry:Event, Medical
Tags:Virtue Insight, pharmaceuticals, clinical trials, clinical research, drug discovery
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