0       0

2019 Webinars


DRI3507 - Preemption in Drug and Medical Device Cases: An Overview and Hot Topics


Jun 20, 2019 12:00pm ‐ Jun 20, 2019 1:00pm

Description

Federal preemption is a key defense in drug and medical device product liability cases, and the FDA’s regulatory framework is the ever-present background factor for our clients and for litigation involving their products. This webinar will provide a brief introduction to federal preemption, aimed at newer lawyers, before shifting to a robust discussion of strategically raising preemption defenses, and will conclude with a forecast of where federal preemption is headed, particularly given the impending changes to the FDA’s 510(k) clearance program.

Objectives:

  • The basics of federal preemption in drug and medical device cases
  • How to strategically raise the defense in a variety of forums, stages of litigation, and fact patterns
  • What’s new on the horizon for federal preemption in drug and medical device litigation, including how changes to the FDA’s 510(k) clearance program could affect the preemption defense.

Speaker(s):

You must be logged in and own this session in order to post comments.

Print Certificate
Review Answers
Print Transcript
Completed on: token-completed_on
Review Answers
Please select the appropriate credit type:
/
test_id: 
credits: 
completed on: 
rendered in: 
* - Indicates answer is required.
token-content
token-speaker-name image
token-speaker-name
token-index
token-content
token-index
token-content
token-index
token-content
token-index
token-content
token-index
token-content
token-index
token-content
/
/
token-index
token-content