Description
The FDA is the gating factor in life science commercialization. Learn about types of market protection you may qualify for and the various expedited reviews– Fast track , Breakthough Therapy, Priority Review. Understand the traditional pathway for drug and device development. Learn how combination products are treated and the difference between and IND and exploratory IND.
Regulatory and Clinical Overview | UCSF Entrepreneurship Center Startup 101 [Full Video]
Yarmela Pavlovic, JD
Meredith Manning, JD
Partners, Hogan Lovells
IN BRIEF:
This video is a compendium of knowledge about FDA and its processes for drugs, devices and diagnostics by two attorneys who specialize in regulatory law.
