Virtue Insight's Clinical Trials Summit 2026

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 - [email protected] 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 – 22nd 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.

Know what’s Happening Next — before everyone else does.

Get App

Host or Publisher Virtue Insight