Health Law Webinar - FDA and Medical Devices

What we'll cover:

  • Manufacturer/establishment registration and medical device listing
  • Device classification, premarket notification 510(k) and premarket approval
  • Investigational Device Exemption (IDE) for clinical studies
  • Quality system regulation and labeling requirements
  • Medical device and adverse event reporting
  • Mobil devices and medical apps

There is no charge for this webinar.

Thursday, May 12, 2016, 12:00-1:00 MT

Location: Webinar Only

Pia Dean, Attorney, Holland & Hart LLP

To register online please click here.

Questions? Contact Susan Westberry at 303-295-8273 or


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