New England: Advanced Topics in Medical Device Regulation

When:  Nov 30, 2016 from 04:00 PM to 06:00 PM (ET)
Associated with  ACRP New England Chapter

Advanced Topics in Medical Device Regulation

View Event Flyer. 

Speaker: Chris Cain, VP, Clinical and Regulatory Affairs, Corindus, Inc.

Registration Cost: Free for all to attend.

Program Agenda:

  • 4:00 – 4:30 pm – Arrival & Networking
  • 4:30 – 6:00 pm – Speaker Presentation

Program Description: 2016 has been a big year for FDA and the release of Guidance Documents (20+ Draft Guidances). Many of which will have a direct impact on clinical and regulatory strategy. During this three Guidances will be discussed in detail.

Upon completion of this program, attendees should be able to:

  • Understand how recent FDA (Draft) Guidances may impact clinical and regulatory strategy.
  • Identify three key elements from each (Draft) Guidance.
  • Learn practical ways of implementing the Guidance through real-world experience

Target Audience: Open to all Clinical Research Professionals

Further Information: Contact Denise Clarke at or call 617.306.5514.

Refund Policy: No refunds provided unless canceled by chapter.

Level: Open to all clinical research professionals.

Contact hours: 1.5 Contact hours have been applied for through ACRP. Membership is not required for online registration of contact hours.

To receive contact hours: Purchase the contact hours, sign in at the registration desk, and attend the program. Log on to the ACRP website then “ACRP Learning Portal” to complete the evaluation no later than 30 days following the event and obtain the online certificate.

Contact Hour Cost:

  • $0 Chapter Members
  • $15 ACRP Members
  • $30 Non-Members

Please click here to purchase contact hours


Constant Contact
1601 Trapelo Road
3rd Floor, Great Room
Waltham, MA 02451
Event Image


Denise Clarke