13th Annual Clinical Trials Summit 2022

Virtue Insight

13th Annual Clinical Trials Summit 2022

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13th Annual Clinical Trials Summit 2022


19th May 2022, Kohinoor Continental Hotel, Mumbai, India


13th Annual Clinical Trials Summit 2022 will provide a platform to discuss on the futuristic advancements in clinical trials and clinical research. This multidisciplinary program involves broad participation of people from clinical trials community from around the globe who are focused on learning more about clinical research, clinical trials planning and management.


This conference intends to focus on the global health and clinical trials around the world. Bioethics, regulations, patient recruitment, site selection, real-world data, data integration & Strategy, outsourcing, vendor management, quality (QbD) in Trial Conduct, risk-based monitoring, clinical auditing & financial planning and other significant topics that play a key role in clinical trials will be addressed along with innovative sessions on new technologies, effective and quality collaborations.




Tenthpin, Clinevo Technologies, Advity Research, Ontime Globe Kyarrier, Innvocept Solutions, Target Institute Of Medical Education & Research, Zuellig Pharma, Chitkara University




E-mail – [email protected]  or Call – + 91 44 24762472/ +91 9361957193

Standard Price   – (INR 15,000 + GST (18%) per delegate)
Conference Sponsor, Exhibition Stall & Paid Speaker Slot – Please email your interest and queries



MUKESH KUMAR, Senior Vice President & Head, Clinical R&D, Cipla
SADHNA JOGLEKAR, Senior Vice President, Global Medical Affairs, Sun Pharma
PRATIK SHAH, Vice President Medical Affairs, Bharat Serums and Vaccines
RAVI SEKHAR KASIBHATTA, Senior Vice President, Clinical Research, Lupin
MANISH SHAH, Associate Vice President, Wockhardt
SANDESH SAWANT, Senior Director, Medical Services Head – Clinical Trials, Cipla
RAGHURAM JANAPAREDDY, Partner & Managing Director – India, Tenthpin
DIVAKAR KOLLI, Associate Director and Head – Clinical & Non-Clinical QA, Cipla
TUSHAR SAKPAL, Director – Clinical Data Standards & Automation, Novartis
MILIND ANTANI, Leader, Pharma and Healthcare, Nishith Desai Associates
YASMIN SHENOY, Director-Regulatory Affairs, Sanofi
ANIKET JOSHI, Associate Global Portfolio Delivery Director, Novartis
RISHI JAIN, Medical Director, AbbVie
DILIP PAWAR, Head – Medical Affairs and Pharmacovigilance, Unichem Laboratories
CHIRAG TRIVEDI, Clinical Study Unit Cluster Head, Sanofi
KEDAR NAYAK, Head – Clinical Development, GSK
ARUN BHATT, Consultant – Clinical Research & Development
AMITA BHAVE, Head Regulatory Affairs GDD, Novartis
HARSHAD KOTHAWADE, Head-Regulatory Management & Trade Compliance, Merck
SADANAND KULKARNI, Head-Medical, Regulatory, Vigilance, Quality, Fresenius Kabi
VAIBHAV SALVI, Head – Medical Information, Asia, Sanofi
INDRANIL PURKAIT, Sr. General Manager and Head Medical Affairs, Ipca Laboratories
ASHWANI PANDITA , General Manager Quality Management & Training, Global Clinical Research Operations, Glenmark
VALLABH DESHPANDE, HOD PV Operations, Glenmark
VISHWAS SOVANI, Founder Director, Pharmawisdom
GANESH KADHE, Senior Leadership Team Member, Scientific & Medical Affairs, Abbott Nutrition
SAKHARAM GARALE, Founder & CEO, Renovare Healthcare Solutions
ROSHAN PAWAR, Associate General Manager, Alkem Laboratories
Plus more joining soon



The growth of hybrid trial and virtual trials in India – Where we are?
Better patient recruitment and retention – Can be achieved by DCT?
Digital transformation and AI in clinical trials
What are key challenges in patient safety? Ways to overcome and better alternatives
Risk-based monitoring (RBM) – Is ensuring patient safety?
Clinical trial design and implementation – How technology makes an easier way?
Wearable devices, remote monitoring and virtual trials – Risk and benefits
Key market trends and challenges driving opportunities and outsourcing
End-to-end strategic partnership and managing the communications gap in CROs
How can sponsors successfully manage the EU CTR change?
Technology accelerates new age clinical research
Are the regulations sufficient in clinical trials and what needs to be done?
Remote clinical research – Risks and chances
How RWE is transforming clinical trials?
How do we deal with privacy concerns around RWD?
Ensuring and maintaining compliance with the rules and regulations.
Be part of a major networking opportunity



CIOs, CEOs, CDOs, Vice Presidents, Presidents, Heads, Directors and Team Leaders from the following areas:


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 System


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.


To register for this event please visit the following URL: https://www.virtueinsight.com/event/clinical-trials/ →


Date And Time

2022-05-19 to

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