Event Description
9th Annual Pharma Regulatory Summit 2026

9TH ANNUAL PHARMA REGULATORY SUMMIT 2026

 

“Driving Regulatory Excellence for a Changing Pharma Landscape”

 

24th March 2026, Hotel Kohinoor Continental, Mumbai, India

 

The 9th Annual Pharma Regulatory Summit 2026 congregates foremost global pharmaceutical industry professionals and regulators to share their insights on technologies, approaches, and solutions that will drive innovation and quality for the medicines delivered to patients worldwide. This interactional setting with expert-led regulatory and industry presentations will ensure pharmaceutical industry professionals to develop and apply ingenious solutions in today’s Indian pharma ecosystem.

 

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

DELEGATE REGISTRATION :

 

Super Early Bird Price (Valid until 06th Feb 2026) – INR 10,000+ GST (18%) per delegate

 

Early Bird Price (Valid from 07th Feb - 13th March 2026) – INR 12,000+ GST (18%) per delegate

 

Standard Price  – INR 15,000 + GST (18%) per delegate

 

SPONSORS:

 

Conference Sponsor – 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
NAGENDRAN IRUKULAPATI,  Sr. Vice President – Global Regulatory Affairs, Aurobindo Pharma
RAMANARAYANA PARHI, Vice President & CIO, Alkem Laboratories

JULIET REBELLO, Director - Clinical Dev Strategy & Medical Writing,Cipla
ANJU AGARWAL, Director Global Patient Safety, Advanz Pharma
AMITA BHAVE, Director Regulatory Affairs, AstraZeneca

MILIND ANTANI, Leader, Pharma and Healthcare, Nishith Desai Associates

PALLAVI TRIVEDI, Associate Director – Diabeties and Obesity, Global Business Services (GBS), Novo Nordisk 

SANTOSH TAUR, Director Medical Affairs, Vaccines, Rare Diseases and Digital, Pfizer

AKSHAYA ODAK, Head Regulatory Affairs (Biotech), Lupin
PROTITI BAGCHI, Associate Director- Digital Transformation, GSK
SUCHITA MORE, Director Medical Modernization, Asia Pacific & Japan, Merck Sharp & Dohme 

AMARNATH SUGUMARAN, Director - Medical Affairs, Cipla  
SHUVANKAR BALLAV, Head, Regulatory Affairs - Advanced Biotech Lab (ABL), Ipca Laboratories
PANKAJ CHAUDHARI, Head - Global Regulatory Affairs (Biosimilar), Abbott
AMOL CHOULWAR, Group Leader - Regulatory Affairs (Biosimilar Peptides New Drugs Vaccines),Cipla 

MINOO BIJU, Head-Regulatory Affairs, Piramal Pharma Solutions
MARTINA GOMES, Head, Reg Affairs – CH, Bayer
PRIYA CHATTERJEE, Head Regulatory Affairs - South Asia, Bayer
SHIRAZ KANDAWALLA, Head – Regulatory, Quality & Safety – India, Ferring Pharma
SADANAND KULKARNI, Head - Medical, Regulatory, Vigilance & Quality (South Asia), Fresenius Kabi
JAYASHRI PRAMOD, Regulatory Principal Specialist, Novo Nordisk
SUSHMITA KUSWA, Head Medical & Regulatory Affairs, Piramal
OMPRAKASH S. SADHWANI, Former Joint Commissioner & Controlling Authority, FDA (Maharashtra State)
RUCHIR SHAH, Head Medical Devices Category, Regulatory & Safety Manager, Reckitt Benckiser
RASHMI HEGDE, Former Executive Vice President – Medical, GSK
NEELU GOEL, Regulatory Affairs - Head Business Continuity & Compliance, Sun Pharma
PRIYA PRASAD, General Manager – PV, Lupin
KAVITA LAMROR, Partner, RWE & Digital Transformation, Maxis Clinical Sciences

 

Plus more joining soon

 

FOCUS AREAS:

  • Digital Transformation
  • Biologics & Biosimilars
  • Regulatory Writing & Submissions
  • Clinical Trials/DCT
  • Patient Safety
  • RWE/RWD
  • New Drugs
  • Generic Groups
  • Vendor Management
  • Medical Devices

 

 WHO SHOULD ATTEND AND WHO YOU’LL MEET:

 

This conference is specifically designed for pharma, biotech, CRO’s, Government and Regulators, Hospitals/Trial Sites, Technology / Solution Providers from following areas;

 

Regulatory Affairs, Clinical Trials / Clinical Data, Biologics & Biosimilars, Medical Devices, Regulatory Writing/Medical Writing/Publishing/Information/Submissions, Document and eRecords Management, Clinical Trials Management/Data, Outsourcing /Vendor Management, Quality Assurance/Quality Control, Technology AI, ML, Blockchain, Big Data, Supply Chain Management , Government- Department of Health, Vaccines R&D / Innovation, Consultants

 

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, and 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 at the high-level conference.

 

End Date
Start Date
Event Speciality
For registration/tickets purchase:
https://virtueinsight.com/events/pharma-regulatory-summit-2026-2/
Currency Symbol:
INR
Event Cost:
15000
Event Types (Select all that apply)
Medical Conference
Event Registration Contact Email
Kavitha@virtueinsight.co.in
Event Information Contact Email
Kavitha@virtueinsight.co.in
CME Credits
No
Exhibits
Abstract Submission Deadline
(+1) 206-575-7771
Medical Events Worldwide
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