10 December 2020
12:30 PM - 2:00 PM EST
Registration for this event has closed
HBA INDIANAPOLIS PRESENTS

Rescheduled: Ask an Expert about EU Medical Device Regulation - Lessons Learned in the Field

Join our EU MDR consultants who are working with industry’s early adopters of the regulation for a question and answer session on the good, the bad, and the ugly they have seen as companies transition. Not sure about how to handle a single-integral combination product or if your co-packaged device falls under the EU MDR or the Medicinal Products Directive? The experts can share their experiences with how the regulation will be applied for combination products. Just re-certified under the EU MDD and concerned about timing for transition to the EU MDR over the next three years. Our team can discuss thoughts on strategy. Put a stop to your interoffice in-decision and chat with an expert.

Once registered, participants will have the opportunity to submit questions by email to the speakers. At the event this team will share initial thoughts on EU MDR implementation, discuss pre-submitted questions, and answer general questions from the audience.

Additional Information 
To pre-submit questions email dorothy.henckel@guidehouse.com. Please include the text "Ask an Expert About EU MDR".

Agenda 
11:30 – 11:40 AM Welcome and introductions
11:40 – 12:10 PM Presentation
12:10 – 12:30 PM Pre-submitted questions answered
12:30 – 1:00 PM Group Discussion and Q&A

Registration information
Event is open to: HBA Members and Nonmembers
Online registration deadline: 10 December 2020

Featured Speakers

Paula Burge
Guidehouse

Pricing

 MemberNon-Member
Regular Registration$10.00 / €9.00$15.00 / €13.00

Members receive up to 50 percent discount



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