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9th Annual Clinical Trials Summit 2018

Individual

9th Annual Clinical Trials Summit 2018

|

activities & events / Professionals
₹ 8260 /Ticket
INFORMATION

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)

MAYUR PARMAR, Deputy Collector, Government of Gujarat

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

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

MILIND ANTANI, Partner In-Charge - Pharma LifeSciences, Nishith Desai Associates

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

RANJIT BARSHIKAR, QbD / CGMP Consulting, Member Editorial Board Journal of Generic Medicines, England

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 24762472

Standard Price  – 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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Venue Description
Andheri Kurla Road, Andheri ( E ), Mumbai 400059 - India , Mumbai, Maharastra, India - 400059
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