9th Annual Pharma Regulatory Summit 2026

Website https://virtueinsight.com/events/pharma-regulatory-summit-2026-2/ | Edit Freely

Category pharma

Deadline: March 23, 2026 | Date: March 24, 2026

Venue/Country: Mumbai, India

Updated: 2026-01-21 15:18:40 (GMT+9)

Call For Papers - CFP

“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 - kavithavirtueinsight.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.