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Basic Documentation Requirements for Compliance under U.S. FDA and EU MDD


Product Format: Live Webinar Presenter(s): John E. Lincoln Conference Date: Tue, Mar 28, 2017 Aired Time: 1 pm ET | 12 pm CT | 11 am MT | 10 am PT
Length: 90 minutes
Price: $227.00

This webinar by expert speaker John E. Lincoln will examine the existing and proposed requirements for the U.S. FDA's DHF - including its derivative documents, the DMR and DHR. It will consider the European Union's MDD TF/DD requirements, and evaluate the documents' differing purposes/goals, as well as the two different device classification schemes.

Special Offer: Use code EVENT25 to get $25 discount.

Not able to attend the audio session? We will provide you with a replay of the session, or you can request a DVD recording.

For any queries feel free to contact Customer Service at 1-866-458-2965.

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