Commercializing medical technology in the US? – Learn about the regulations before you start.

June 17, 2021 @ 8:00 am CST

Join us for complimentary webinar tailored to pharmaceutical and medical technology manufacturers entering the US Market, followed by Q&A.


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Date: Thursday, June 17th, 2021, 8:00 – 9:00am CST, 3:00 PM-4:00 PM (UTC+01:00) 

Join US attorneys with FDA regulatory, quality, and privacy expertise to learn about:

  • Key FDA regulations related to quality system and submissions, recent enforcement trends, best practices, and pitfalls to watch out for.
  • HIPAA privacy requirements for drug and device makers and differences (and similarities) between HIPAA and GDPR.

Speakers:

Amanda Johnston Paul Rothermel


Sponsored by:

 

 

 


Attendees include Pharmaceutical and Medical Technology Manufacturers interested in learning about recent changes & implications, and in particular, those working in Compliance, Legal, Finance, Regulatory & Operations. CLE credits – Application pending in various jurisdictions. Please contact Tracy at terickson@gardner.law with any questions.