8th Annual Pharma Regulatory 2025

8th Annual Pharma Regulatory 2025

“Recent regulatory developments – What’s the way forward?”

11th March 2025, Kohinoor Continental Hotel, Mumbai, India

The 8th Annual Pharma Regulatory Summit 2025 brings together leading global pharmaceutical industry professionals and regulators to exchange insights on cutting-edge technologies, strategies, and solutions that drive innovation and uphold quality in medicines delivered to patients worldwide. This interactive forum features expert-led presentations and discussions, creating an ideal platform for professionals to explore and implement innovative solutions tailored to the evolving regulatory landscape of India’s pharmaceutical industry.

Please contact Email - bookings@virtueinsight.com or Call - +91 44 42108101/ M: +91 9361957193 

DELEGATE REGISTRATION:

Super Early Bird Price (Valid until 28th Jan 2025) –  INR 12,000 + GST(18%) per delegate

Standard Price  – INR 17,000 + GST(18%) per delegate

SPONSORSHIP:

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

ZOHER SIHORWALA, Senior VP & Head – Global Regulatory Affairs, Wockhardt

SUYOG MEHTA, Sr. VP & Head – Medical Affairs & Clinical Research, Sun pharma

PRABIR KUMAR PAL, Senior VP - Quality & Compliance, Alkem Laboratories

RAMANARAYANA PARHI, Vice President & CIO, Alkem Laboratories

GEETA SHANBHAG, VP - Pharmacovigilance and Medico-regulatory Affairs, Ipca Laboratories

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

ANAND SAXENA, Director - Regulatory Affairs, Cipla

AMARNATH SUGUMARAN, Associate Director & Cluster Head Medical Affairs, Cipla

AMIT PANDEY, Executive Vice President & General Counsel, GSK

SAILESH YHNB, Associate Director, RA Device Established Products, Novo Nordisk

YASMIN SHENOY, Senior Director - Regulatory Affairs, Sanofi

SHIRAZ KANDAWALLA, Associate Director - Regulatory Affairs, Ferring Pharma

SOURABH FULMALI, Global Medical Director, GSK

SAURABH THUKRAL, Cluster Head- Centre of Excellence, Dr. Reddy Laboratories

RISHI JAIN, Country Medical Head, Novartis

SRINIVASAN ACHARY, Associate Director, Pfizer

RASHMI HEGDE, Former Executive VP – Medical, GSK

PRIYESH MISTRY, Head - QA/21CFR Compliance, Intas Pharmaceuticals

SWEETY MATHEW, Regulatory Professional, RA CMC Biotech & Rare Disease, Novo Nordisk

AMOL DESHPANDE, DGM Technology Transfer, Emcure Pharmaceuticals

MAYUR MAYBHATE, Head Medical Affairs, Alkem Laboratories

SADANAND KULKARNI, Head- Medical, Regulatory, Vigilance & Quality South Asia, Fresenius Kabi

PRIYA KANAKIA, Head - Safety Writing, Lupin

ROSHAN PAWAR, Head Medical Affairs, Alkem Laboratories

GOPINATH MADHU, Senior Client Partner, Digital & Technology, Pfizer

OMPRAKASH S. SADHWANI, Former Joint Commissioner & Controlling Authority, FDA (Maharashtra State)

KRUPA BAHEKAR, General Manager, Emcure Pharmaceuticals

MARTINA GOMES, Head, Regulatory Affairs – CH, Bayer

NEELU GOEL, Regulatory Affairs - Head Business Continuity & Compliance, Sun Pharma

MANGALA KOTNIS, Former Head Regional Medical Affairs (MSL/ FME function), Abbott

PRASHANT BODHE, Director, CliniSearch

VARSHA NARAYANAN, Founder-Director, Dr Varsha’s Health Solutions

Plus more joining soon

FOCUS AREAS THIS YEAR:

Regulatory concerns focusing on following areas

Regulating pharma in India

RWE / RWD

Medical Devices

Biosimilars

Clinical Trials / DCT

Audits / Inspection

Regulatory Submissions

Digital Era – AI, ML, DA

Digitalisation

Regulations for Prioritising patients

Drug registration compliance

What’s the way forward

Opportunity - Learn & Network

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, and medical device professionals responsible for Regulatory info from following areas

Regulatory Affairs, Regulatory Writing/Medical Writing/Publishing/Information/Submissions/Audits & Inspections, Document and eRecords Management, Drug Safety, Clinical Trials Management/Data, Biosimialrs, Clinical Dat, Outsourcing/Clinical Outsourcing/Vendor Management, Product Development, Quality Assurance/Quality Control, Patient recruitment companies, Gov - Department of Health, Non-profit organizations/ Association, Consultants

Maximize your experience at the event with a broader scope that brings the entire communications value chain together. Take advantage of dedicated networking sessions to connect with industry leaders and explore cutting-edge innovations from leading international vendors in the co-located exhibition. Enhance your expertise by gaining insights into the latest business models and strategies at our high-level conference, designed to empower and inspire professionals across the sector.