This webinar will examine the requirements 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. It will evaluate the documents' differing purposes / goals, as well as the two different device classification schemes. Required and desirable contents will be discussed. Also considered: Areas requiring frequent re-evaluation / update; Similarities and differences; Future trends; Typical DHF / D&DP Table of Contents;  Technical Documentation Table of Contents; The importance and usefulness of the new "General Safety and Performance Requirements" of the EU MDR; Structure of the "Declaration of Conformity"; self-declaring or N-B reviewed;  Parallel approaches to development. Finally, the differing approaches to device file audits by the FDA and the Notified Body will be discussed.

One of our most popular webinars, continuously updated with the latest U.S. FDA and Eurpean  Union requirements. As U.S. companies go global, they must meet different product design documentation.  The cGMPs mandate Design Control and the Design History File (DHF). EU / ISO 13485 mandate Design and Development Planning and File.  In order to sell globally, the EU's CE-marking documentation is a requirement -- the Technical FiIe or Design Dossier under the old EU MDD, and the Technical Documentation requirements of the new EU MDR.  Currently they serve different purposes, support different goals, but there are steps toward harmonization.  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, and understand the new EU MDR documentation requirements.