17th Annual Clinical Trials Summit 2026

“Bridging Innovation & Integrity: Shaping the Future of Patient-Centric Clinical Trials”

10th & 11th June 2026, World Trade Center (WTC), Mumbai

The 17th Annual Clinical Trials Summit 2026 will serve as a premier platform to explore future advancements in clinical trials and research. The multidisciplinary program brings together professionals from across the clinical research ecosystem to discuss trial planning, management, and emerging innovations. The summit fosters collaboration among industry, academia, patient advocacy groups, and regulatory bodies to address real-world challenges in trial design, data analysis, and execution. Through focused discussions on innovative strategies, new technologies, and quality partnerships, the event aims to advance patient-centric and efficient clinical research.

Sponsor / Delegate Registration E-mail - kavitha@virtueinsight.co.in or M: +91 9361957193

DLELEGATE  REGISTRATIONS:

Exclusive Deal: 3 for the Price of 2! - Limited time offer with limited seats only.
 
Super Early Bird Price (Valid until 10th April 2026) - INR 15,000 + GST per delegate

Early Bird Price (Valid from 11th Apr – 22^nd May 2026) - INR 15,000 + GST per delegate
 
Standard Price  (Valid from 23rd May 2026)  - INR 19,000 + GST  per delegate

PARTNERSHIP:

Exhibitor  - Aeris Dynamics

Conference partner – Should you wish to Sponsor, or purchase a Exhibition Stall (Booth) / paid Speaker Slot / create brand awareness, you can simply email or call your interest and queries.

KEY SPEAKERS:

MAYUR PARMAR, Drugs Inspector (Deputy Collector, Gujarat Government), FDA
SHUBHADEEP SINHA, SVP, Head - Clinical Development & Medical Affairs (CD&MA), Hetero Labs
RAMESH JAGANNATHAN, VP, Medical Dept, Clinical Research & PV, Bharat Serums and Vaccines
ANIL KUKREJA, Executive VP - Clinical Research & Medical Affairs, Emcure Pharmaceuticals
SHALINI MENON, Executive VP Medical Affairs, GSK
RAJENDRA KUMAR KASI, VP & Global Head – Pharmacovigilance, Glenmark Pharmaceuticals
MILIND ANTANI, Leader, Pharma and Healthcare,Nishith Desai Associates

RAMANARAYANA PARHI, VP & CIO,Alkem Labs
RUTEJA JOGLEKAR, Director Site Management & Monitoring, AstraZeneca Nishith Desai Associates
SHAILENDRA SACHAN, Director - Clinical Operations,Teva Pharmaceuticals

PRABHAT SINHA, Director Government & Public Affairs, Boehringer Ingelheim
RAJESH KHER, Director, Integrated Business Operations, Janssen Pharmaceutical
SANTOSH TAUR, Director Medical Affairs - Vaccines & Digital, Pfizer
VAIBHAV SALVI, Director & Head – Clinical Study Unit, India & South East Asia,Sanofi
KEDAR SUVARNAPATHAKI, Director Regulatory Affairs - Southeast  Asia & India, Johnson & Johnson

KEDAR NAYAK, Director - Global Study Management, GSK
SIVA KUMAR BUDDHA, Medical Director Global Patient Safety,Amgen
JAMAL BAIG, Director Drug Safety, MSD
SWAPNALI RAUT, Director, Global Clinical Operations, GSK

ANUPRITA SHETH, Associate Director Vendor Oversight Lead,Kenvue
MOHIT TRIVEDI, Country Safety Head India, Sanofi
EMRAN KHAN, Global Clinical Operations Leader, Trial Governance, Strategic Outsourcing, Sun Pharma

DIVAKAR KOLLI, Director - Development Quality Assurance,Cipla
SUCHITA MORE, Director V&I Medical Modernization,MSD

SOURABH FULMALI, Global Medical Director – Respiratory, Allergy, CVS, GSK
RISHI JAIN, Country Medical Head, Novartis
AMARNATH SUGUMARAN, Associate Director & Cluster Head Medical Affairs, Cipla
PROTITI BAGCHI, Associate Director - Global lead for Content & Marketing Operations and CX | Digital Transformation,GSK
BAIDYANATH MISHRA, Head- R&D Healthcare, Medical Affairs & Clinical Research,Dabur

DYOTONA SEN, Head - Medical Affairs & Clinical Research, Galderma
KAPIL MEHTA,  Head Medical Affairs,JB Pharmaceuticals
JYOTSNAPATWARDHAN, Cluster Head Clinical/PV Country Quality Middle East/Africa/Turkey/India,Novartis
MARTINA GOMES, Head, Reg Affairs – CH,Bayer
K. MURUGANANTHAN, Head - Study & Site Operations(SSO India), Global Clinical Operation(GCO), Novartis
KHOKAN DEBNATH, Head of Regulatory Affairs, Clinical Operations & Pharmacovigilance, Wockhardt
PANKAJ THAKUR, Sr GM & Head Project Management,Hetero Labs
AKSHAYA ODAK, Head Regulatory Affairs (Biotech), Lupin

RENUKA NEOGI, Head & Deputy GM – Global Clinical Quality Management,Sun Pharma
MAYUR MAYBHATE, Head Medical Affairs, Alkem Laboratories
OMPRAKASH S. SADHWANI, Former Joint Commissioner & Controlling Authority, FDA (Maharashtra State)
RASHMI HEGDE, Former VP Medical Affairs, GSK
ASHWANI PANDITA, Sr. GM Quality Management & Training, Global Clinical Research Operations, Glenmark Pharmaceuticals
PRASHANT MEHROTRA, Senior GM - Clinical Research, Bharat Serums and Vaccines
SHRADDHA BHANGE, Senior Medical Safety Lead, Sandoz
RANJIT BARSHIKAR, CEO, QBD International, United Nations Adviser
PARIMA DALAL, Clinical Scientist ( Manager), Clinical Research Group, Torrent Pharma
HARSHAD KOTHAWADE, Former Head of Regulatory Management & Trade Compliance, Merck Group
NEELAKANT KRISHNAN, Sr. GM - Head Global Trial Management, Sun Pharma
KAVITA LAMROR, Partner, RWE & Digital Transformation, Maxis Clinical 
MANGALA KOTNIS, Former Head Regional Medical Affairs, Abbott 

AMANDEEP KAUR TENEJA, Global Aggregate Reporting & RMP Manager, Kenvue

PRIYANGSHU CHOWDHURY, Centralized Monitoring (RBQM), GSK
BISMITA BORKAKOTY, Central Monitoring Associate, GSK

Plus more joining soon

KEY THEMES FOCUSED ON THIS CONFERENCE:

Clinical Trials - Market Analysis - Opportunities & Challenges
Decentralised Clinical Trials (DCTs
Patients Prioritised Trials
Work Together - Sponsor / Site / CRO/Patients / Regulators
Outsourcing / Partnerships
Clinical Trail Management
RWE & RWD
Key Regulatory Changes & Developments
Innovative methods for Clinical Trial Design
Inspection Readiness / Site Management / Risk Monitoring
Clinical Trial Supply - What's the new way forward?
Technology & Innovation: Transforming clinical trials

WHO SHOULD ATTEND AND WHO YOU’LL MEET:

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.