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Planning for success: When and how to develop a regulatory roadmap

Regulatory approval is a major inflection point and value driver for companies, yet many wait too long to plan and develop a roadmap for success. In this workshop you will learn about:


  • The overall regulatory process
  • What steps to take and when to take them
  • Documentation and quality systems
  • What to look for in hiring regulatory expertise


Our speakers have first-hand experience and expertise in all phases of the regulatory process for drugs and IVD/devices. Regardless of the stage of your company, you will gain valuable knowledge and insights. Join us for an informative discussion.



Jennifer Grodberg, Sr. Vice President, Regulatory Affairs and Program Management, Forge Therapeutics

Luis Jimenez, Vice President, Business Development, Brandwood Biomedical

Michael Monahan, Sr. Director, Regulatory Affairs and Quality Assurance, Crinetics Pharmaceuticals



5:30pm –  6:00 pm Networking and light refreshments

6:00pm –  7:30 pm Presentations and Q & A

7:30pm –  8:30 pm Breakout Sessions with individual speakers / discussion & networking


$30 SDEE & HeraHub Members

$50 Non-members

October 09, 2018 at 5:30pm - 8:30pm
Hera Hub
4010 Sorrento Valley Blvd
Suite 400
San Diego, CA 92121
United States
Google map and directions
Danielle Hayes ·

Will you come?

$50.00 Regulatory Roadmap Non-Member Ticket
$30.00 Regulatory Roadmap Member Ticket

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Global Life Sciences Practices Group


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SDEE is a nonprofit 501(c)(3) organization founded by local San Diego entrepreneurs
in order to provide a voice for the early stage start-up, to support new entrepreneurs and their companies,
and to sponsor networking and educational events
to help develop the skills necessary to bring funding, business, and jobs to the San Diego area.

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