9th Annual Pharma Regulatory Summit - 2026, Hotel Kohinoor Continental, Mumbai, Maharashtra, India.
Virtue Insight was founded in 2009. We equip business professionals around the world with the latest in-depth industry knowledge and provide networking opportunities in telecom, technology and pharmac...
About the Event
Virtue Insight was founded in 2009. We equip business professionals around the world with the latest in-depth industry knowledge and provide networking opportunities in telecom, technology and pharmaceutical industries. Our aim is to provide a platform to share knowledge, insight and provide our clients to network effectively and deliver maximum ROl by making new business alliances. We strive to produce high quality conferences that include the latest topics which are delivered by world class leaders of the industry. We are based out in India, USA and UK
Highlights
We believe in gathering information from all possible sources and try to be at top as possible. Our clients trust us on being capable of "staying ahead" with this competitive market .As we grow very fast with new opportunities, we welcome our new team members on regular intervals and provide them with lots of opportunities to expand their horizon.As the technology is taking a vast space, we provide assistance with new ideas and thoughts to our stakeholders. We work with the lastest technology with updated and empowered thought process.We believe in providing the best comfort by understanding the client's need through our friendly culture. We have a win-win relationship with all our customers in place.
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Coffee and Registration
Tuesday, 24 Mar 2026Coffee and Registration
Coffee and Registration
Welcome Address & Opening Remarks
Welcome Address & Opening Remarks
Regulatory Roadmap for Generics:
Compliance Strategies for a Competitive Market Global regulatory updates shaping new drug development Early regulatory engagement and scientific advice pathways Streamlined clinical development and accelerated approval routes Ensuring safety, immunogenicity, and quality standards Strengthening CMC and manufacturing compliance Global health priorities and pandemic-readiness frameworks End-to-end patient safety and post-market surveillance
| Time | Type | Title | Speaker(s) | Venue / Room | Notes |
|---|---|---|---|---|---|
|
8:30 AM 9:00 AM |
Opening Ceremony | Coffee and Registration | – | – | Coffee and Registration |
|
9:20 AM 10:00 AM |
Opening Ceremony | Welcome Address & Opening Remarks | – | – | Welcome Address & Opening Remarks |
|
9:30 AM 10:00 AM |
Session | Regulatory Roadmap for Generics: | – | – | Compliance Strategies for a Competitive Market Global regulatory updates shaping new drug development Early regulatory engagement and scientific advice pathways Streamlined clinical development and accelerated approval routes Ensuring safety, immunogenicity, and quality standards Strengthening CMC and manufacturing compliance Global health priorities and pandemic-readiness frameworks End-to-end patient safety and post-market surveillance |
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