7th Annual Clinical Trials Summit 2016

7th Annual Clinical Trials Summit 2016
24th May 2016, The Lalit Hotel, Mumbai, India

“A critical guide for successfully conducting clinical trials”

KEY THEMES DISCUSSED IN THIS CONFERENCE:-

-Insights, Implications, Impact and Implementation of risk management in trial conduct
-Tracking returns, Reconciliation & Destruction to manage costs
-Reduce significant costs through successful embedding of modulation and simulation in the clinical supply chain
-Underlining the benefits and implications of drug pooling in the clinical supply chain
-Marketing for your clinical research practice
-Insurance coverage: How the ACA changed access to clinical trials
-Regulatory updates and Good Clinical Practice (GCP) auditing techniques
-Developing a standardized tool to improve patient comprehension during consent
-Insight and practical tips on how to work with all payer types to obtain coverage of clinical trial routine costs.
-ACA, Medicare, Medicaid and state requirements regarding coverage of clinical trials.
-Update yourself with respect to terms of legislation, policies, systems, technology, communication strategies and best practices
-Maintaining proper balance in relationships: Sponsor – Site – CRO & Patients
-Overcoming challenges faced in regulatory approval processes – obtaining drug/ clinical supplies import and export licenses in Asia
-Margin of safety: Identifying ideal clinical sites and strategizing patient recruitment and clinical sites management in India to develop appropriate clinical studies
-Next generations of clinical trials – How big will the market be?
-Be part of a major networking opportunity

KEY SPEAKERS:-

• John Lambert,Chief Medical Officer Early Phase, PAREXEL International (UK)
• SumitMunjal, Medical Driector Lead- Global Medical Saftey, Head Of Mature Established Products, Takeda Pharmaceuticals(UK)
• Arun Bhatt, Consultant- Clinical research & Development
• BhaswatChakaraborthy, Senior VP & Chair, Research development Core Committee, Cadila
• Anish Desai, Director medical affairs, Clinical Operations Device safety, Jhonson&Jhonson
• Hema Bajaj, Head Of Clinical Quality & Medical Compliance, Affiliate Quality Officer, Safoni Aventis
• SambitPitnaik, CEO Medical Director, Clintech India
• KedarSuvarnapathaki, Head- Regulatory Affiars, BoehringerIngelheim
• Chandra Sekhar, Vice Peresident Quality (Pharma), Ralaiance Life Sciences
• NareshTondare, Head- India & Nepal Regulatory Affiars, Glenmark Pharmaceuticals
• MurtuzaBughediwala, Associate Director, Project Mabagement& Strategic Initiatives, Sanofi
• ShilpaRaut, Regional Training Head- Asia, Middle East& Africa Cluster, Novartis
• DeeptiShangavi, Assisstant Manager, Medical Writing, Tata Consultant Services.
• Amey Mane, General Manager- Medical Affiars, Janssen India (Pharmceuticals Companies Of Jhonson&Jhonson)
• SanketSawant, Strategy & Business Development Partner, SIRO Chinpharm
• AshwaniPandita, Dy. Generam Manager Quality Management & Training, Global Clinical Research Operations, Glenmark Pharmaceuticals
• MilindAntani, Partner in-Charge- Pharmalife Sciences, Nishith Desai Assiciates
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

WHY SHOULD YOU ATTEND?

7th Annual Clinical Trials Summit 2016 - “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:-

-Early Bird Discounted Price - 1 Delegate Pass (INR 6,000 + Tax (14.5%) per delegate) - Book and Pay before 09th April 2016 to avail the early bird discounted price.
-Standard Price (10th April 2016 Onwards):- 1 or 2 Delegates - (INR 7,000 + Tax (14.5%) per delegate) -
-Group Discounts – 3 or 4 Delegates - (INR 6,500 + Tax (14.5%) per delegate)
-Group Discounts – 5 and above Delegates - (INR 5,500 + Tax (14.5%) per delegate)
-Spot Registration on the day of the Conference – 1 Day Conference - (INR 8,000 + Tax (14.5%) per delegate)
-Conference Sponsor & Exhibition Stall – Should you wish to Sponsor, or purchase aExhibition Stall (Booth) or a paid Speaker Slot, you can simply email your interest and queries to us

You can simply email or call and book your conference delegate seats and sponsorships on – TEL: +91 44 64536444. Email – amar@virtueinsight.co.in
We also have some 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.

Virtue Insight equips business professionals around the world with the latest indepth industry knowledge and provides networking opportunities in the telecom, technology, oil and gas, social media, infrastructure and pharmaceutical industry. Our aim is to provide a platform to share knowledge and insights and provide our event attendees to network effectively and deliver maximum ROI by make new business alliances. We strive to produce high quality conferences which include the latest topics which are delivered by world class leaders of the industry.

-Virtue Insight
-Plot No - 07 - 2nd Floor Ekambaram Industrial Estate Alapakkam,Porur Chennai 600 116 India
- +91 44 64536444

This release was published on openPR.