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

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.

This webinar will examine the existing and proposed requiements for the U.S. FDA's DHF - including its derivitive documents, the DMR and DHR. It will consider the European Union's new MDR Technical Documentation requirements, which replace the old Technical File / Design Dossier. It will evaluate the documents' differing purposes / goals, as well as the two different device classification schemes, and CE-marking requirements. Required and desirable contents will be discussed.