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Global Pharmaceutical Regulatory Affairs Summit
22-24 October 2024
Sheraton Brussels Airport, BrusselsHybrid Event

Beverly Chin
Senior Regulatory Submission Manager at Genentech


Beverly Chin is a Senior Regulatory Submissions Manager in the Regulatory Data and Content Chapter within Product Development at Genentech/Roche. With over 23 years focused on Regulatory Submissions, she brings a wealth of expertise in Global Submission Management. Beverly has deep knowledge of drug application filings, and has been at the forefront of many pioneering initiatives like the US FDA’s RTOR (Real-time Oncology Review), Project Orbis and STAR Pilot Program (Split Real Time Application Review). In recent years, she has been involved in several data package pilots with the US FDA in R.

Agenda Sessions

  • Multi-Stakeholder Perspective: Preparing a Global Submission

  • Industry Case Study: Submitting under Project Orbis