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Clinical Trials Summit 2018 : 9th Annual Clinical Trials Summit 2018

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Link: http://www.virtueinsight.com/pharma/9th-Annual-Clinical-Trials-Summit-2018/
 
When May 22, 2018 - May 22, 2018
Where Kohinoor Continental Hotel, Mumbai, Indi
Submission Deadline May 21, 2018
Notification Due May 21, 2018
Final Version Due May 21, 2018
Categories    pharma   biotechnology   clinical trials
 

Call For Papers

9th Annual Clinical Trials Summit 2018
“A critical guide for successfully conducting clinical trials”
22nd May 2018, Kohinoor Continental Hotel, Mumbai, India
Virtue Insight welcomes you to attend the 9th Annual Clinical Trials Summit 2018, which is going to be held in Mumbai on 22nd May 2018. We cordially invite all the participants who are interested in sharing their knowledge and research in the arena of Clinical Trials. 9th Annual Clinical Trials Summit 2018 anticipates participants around the globe with thought provoking Keynote lectures, Oral Presentations and Poster Presentations. This is an excellent opportunity for the delegates from Universities and Institutes to interact with the world class Scientists. The main theme of the conference is to positively learn and educate about clinical trials is essential, if only to counter more negative perceptions.
KEY SPEAKERS:
• OMPRAKASH S. SADHWANI, Joint Commissioner (Nashik Division), Food and Drugs Administration (M.S.)
• K. BANGARURAJAN, Joint Drugs Controller (INDIA), CDSCO (HQ)
• NILIMA A. KSHIRSAGAR, National Chair Clinical Pharmacology, ICMR Govt. of India
• MUZAFFAR AHMAD, Member Strategic Advisory Board on Health Millenium Alliance (Govt of India) and Member Council of India
• JAMILA JOSEPH, Senior Vice President and Head Clinical Research Services, Reliance Life Sciences
• DEVEN V PARMAR, Vice President & Head Clinical R&D, Cadila Healthcare
• ARUN BHATT, Consultant - Clinical Research & Development
• SANDESH SAWANT, Director and Head Clinical Trials, Cipla
• CHIRAG TRIVEDI, Director & Head of Clinical Study Unit, Sanofi-aventis
• DILIP PAWAR, Director and Head - Clinical Development and Medical - Emerging Market including APAC, Merck Sharp & Dohme
• SHIRAZ KANDAWALLA, Associate Director - Regulatory Affairs, Abbott
• BINDU AJIT, Program Director, Biocon Academy
• AMMAR RAZA, Country Medical Director & Chief Medical Office, Allergan
• KEDAR SUVARNAPATHAKI, Head - Regulatory Affairs & IP, Boehringer Ingelheim
• SIDDHARTH DESHPANDE, Assistant Professor Department of Clinical Pharmacology, KEM Hospital
• AGAM SHAH, Head Clinical Operations, Wockhardt
• JYOTSNA PATWARDHAN, Head Development QA, Novartis
• CHIRAG TELI, Head of Medical Services, Alkem Laboratories
• AMEY MANE, General Manager - Medical Affairs, Janssen India (Pharmaceutical companies of Johnson & Johnson)
• SUJAY SURESH KULKARNI, Senior Manager - Medical and Regulatory Affairs, GSK
• PRANJAL BORDOLOI, AVP - Medical Affairs and Pharmacovigilance, Veeda Clinical Research
• PRASHANT BODHE, Director, CliniSearch
KEY THEMES:
• Current challenges and regulations for clinical trials in India
• Having a positive impact on overall market to globalize trials and growth in new product development in emerging countries
• Formulating a risk-based inspection plan for advanced clinical trials
• New tools and technologies for data capture for clinical trials
• Developing effective partnerships and vendor relationships
• Necessary strategies to implement the maximize value of the collaboration.
• Patient and clinical site centricity: Optimising the end users, patients and the clinical sites
• Encouraging data analytics for next-generation clinical trials
• EHR (Electronic Health Records) for clinical research facility
• Recent guidelines issued by FDA on the use of EHR data
• Major roles of clinical pharmacology in drug discovery and development
• New clinical trials rules and its impact
• Current requirements of Indian Clinical Trial Application (CTA) and how this will change with the new clinical trial regulation
• Regulatory considerations in India and south-east Asia
• Be part of a major networking opportunity
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
CONFERENCE REGISTRATION:
Email- kavitha@virtueinsight.co.in Or Call- +91 44 42108101
• Early Bird Discounted Price (Until 4th April 2018) – 1 Delegate Pass - (INR 6,000 + GST (18%) per delegate
• Standard Price (5th April 2018 Onwards) – 1 or 2 Delegates - (INR 7,000 + GST (18%) per delegate)
• Group Discounts – 3 or 4 Delegates - (INR 6,500 + GST (18%) per delegate)
• Group Discounts – 5 and above Delegates - (INR 6,000 + GST (18%) per delegate)
• Spot Registration on the day of the Conference – 1 Day Conference - (INR 8,000 + GST (18%) per delegate)
• Conference Sponsor & Exhibition Stall( Booth) or a paid Speaker Slot are also available.
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 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.

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