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About this Webinar

This is an insightful exploration of Generative AI and its transformative impact on regulatory affairs within pharma R&D.

This webinar delved into the capabilities of Generative AI, shedding light on its relevance in today's dynamic technological landscape.

Expert speakers shared valuable insights into how the pharmaceutical industry is harnessing the potential of GenAI, with a specific focus on regulatory affairs within pharma R&D.

Why Should You Watch This Webinar?

  • Explore GenAI in pharmaceuticals R&D, emphasizing regulatory affairs and medical writing. 
  • Learn about GenAI's impact on regulatory processes, documentation workflows, and compliance,  
  • Discover opportunities to integrate GenAI into existing pharmaceutical and regulatory frameworks.

3 things you'll take away from this webinar

  • Patient Data Redaction: Explore the advanced techniques of safeguarding patient privacy through Generative AI and learn how it's reshaping data redaction practices in the pharmaceutical sector.

  • Regulatory Document Workflows: Gain insights into how Generative AI streamlines and enhances regulatory document workflows, ensuring efficiency and compliance throughout the drug development lifecycle. 

  • Regulatory Compliance: Delve into the critical aspect of regulatory compliance and discover how Generative AI plays a pivotal role in meeting and exceeding regulatory standards.

Who is this webinar for?

This webinar is a perfect platform for Pharmaceutical Researchers and Developers, Regulatory Affairs Professionals, Data Scientists and AI Enthusiasts, and Healthcare Technology Innovators.  

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Know your speakers

Scott Sawler, JD, RPh

Scott Sawler

Former DG of Marketed Health Products Directorate, Health Canada


Nutan B.

Vice President - Consulting at Gramener - A Straive Company

Session moderator

Santosh Shevade

Santosh Shevade

Principal Data Consultant at Gramener - A Straive Company