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