How to Respond Effectively to a Form FDA-483 or Warning Letter
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When: 11/20/2014
2-3pm ET
Where: Member Only Webinar
Presenter: King & Spalding LLP
Contact: Sheri DeVinney

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On Thursday, November 20th, at 2:00pm ET, MDMA will be hosting a member-only webinar, "How to Respond Effectively to a Form FDA-483 or Warning Letter: Best Practices and Common Pitfalls," hosted by King & Spalding, LLP.

Form FDA-483s and Warning Letters are becoming increasingly rigorous and complex, and failing to respond effectively can have serious consequences for device manufacturers. This webinar will:

  • Step participants through the process of preparing an effective response to form FDA-483s and Warning Letters;
  • Identify strategies for avoiding common pitfalls that firms encounter when preparing a response; and
  • discuss the potential implications of failing to submit an effective response

MDMA Members can view the archived audio version of this webinar by clicking here.