Design History Files (DHF), Device Master Records (DMR), Device History Records (DHR), Technical Documentation Files - The US FDA and EU MDR Requirements
In this Interactive presentation, John E Lincoln will discuss the latest U.S FDA and European Union Regulatory Requirements on Design History File, and Technical File/Design Dossier.
Design History Files (DHF), Device Master Records (DMR), Device History Records (DHR), Technical Documentation Files - The US FDA and EU MDR Requirements will be held in Fremont,United States on date 2020-09-08
Deadline for abstracts/proposals : 8th September 2020