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6-Hour Virtual Seminar on The DHF, DMR, DHR, EU MDR Technical Documentation Similarities

October 2 @ 8:00 am - 2:00 pm CDT

$445

Overview

One of our most popular webinars, continuously updated with the latest U.S. FDA and Eurpean  Union requirements. Now expanded to a six-hour format. As U.S. companies go global, they must meet different product design documentation. The cGMPs mandate Design Control and the Design History File (DHF). In order to sell globally, the EU’s CE-marking documentation is a requirement – the Technical FiIe or Design Dossier under the old MDD, and the Technical Documentation requirements of the new MDR.  Currently they serve differnt purposes, support different goals, but the TD File is moving in the direction of the DHF.

And the DHF is adapting to some of the features of the TDFile.  And how / where do the DMR and DHR fit?   Being aware of the similarities and differences in the files and their individual documents can further concurrent development and/or updates to both.

Organizer

94539
Phone:
18003851627
Email:
hrtrainonline@gmail.com
Website:
https://hrtrainonline.com

Venue

Online Event
Ijona Skills,364 E Main Street, Suite 1009
Middletown,DE,USA, DE 19709 United States
+ Google Map
Phone:
+1 3028303132
Website:
https://www.ijonaskills.us/webinarDetails?webinarid=794&speakerid=204&domain=4&source=cc_ln