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Event

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

Speaker:
Pia Dean, Attorney, Holland & Hart LLP

To register online please click here.

Questions? Contact Susan Westberry at 303-295-8273 or sdwestberry@hollandhart.com.

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Unless you are a current client of Holland & Hart LLP, please do not send any confidential information by email. If you are not a current client and send an email to an individual at Holland & Hart LLP, you acknowledge that we have no obligation to maintain the confidentiality of any information you submit to us, unless we have already agreed to represent you or we later agree to do so. Thus, we may represent a party adverse to you, even if the information you submit to us could be used against you in a matter, and even if you submitted it in a good faith effort to retain us.

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