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FDA Regulatory Due Diligence in Mergers and Acquisitions for Medical Device Companies



 
Our Price: $395.00

Product Code: WB-7266
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About the Product
Includes 1 Hour Windows Media Video File and PowerPoint presentations for immediate download.

Whether your company is acquiring other device companies, or itself may be acquired, it is critical to understand the process and best practices for FDA regulatory due diligence. The presenters have counseled companies on numerous transactions involving medical devices, including conducting FDA regulatory due diligence for firms contemplating making an acquisition, as well as preparing acquisition targets for the types of diligence inquiries they may receive and how to respond. We will cover:

  • Best practices and avoiding pitfalls when conducting FDA regulatory due diligence
  • How to craft effective “reps and warranties”
  • Integration and managing post-acquisition risks

Speakers:
Pamela F. Forrest
Partner
Covington & Burling LLP

Scott D. Danzis
Partner

Covington & Burling LLP


Participants that will find this webinar most beneficial will be those involved in medical device companies. Job titles of attendees that will be most applicable for this session will be:
  • Regulatory Affairs
  • Due Diligence
  • Compliance

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