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The DHF, DMR, DHR, EU MDR Technical Documentation Similarities

The DHF, DMR, DHR, EU MDR Technical Documentation Similarities 2025

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Monday, April 25, 2022 - Apr 26, 2022 (2 days), Fremont, United States

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Overview

Date: from Apr 25, 2022 to Apr 26, 2022 (2 days)

Venue Online , Fremont, United States

Organizer Net Zealous LLC - DBA GlobalCompliancePanel

Expected number of attendees : 100

One of our most popular seminars, 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 d...o 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. https://www.gcplearning.com/virtual-seminar/6-hour-virtual-seminar-on-the-dhf,-dmr,-dhr,-eu-mdr-technical-documentation-similarities,-differences-and-the-future-11491LIVE Read more

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Attendees

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John Robinson

John R.

Event organizer

organizer

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