A History of Medical Device Regulation - FDA
Medical device regulation (FDA)
Changes in Europe’s Medical Device Regulations: Consequences for Manufacturers
FDA Product Regulations Part 1 of 7
When should you apply the MDR in Europe ? [Medical Device Regulation]
Documentation Deconstructed: Understanding the Technical file
Device History Record vs. Device Master Record l 21 CFR 820 DHR DMR l The Learning Reservoir
How is CDRH Structured?
IMDRF - International Medical Device Regulators Forum
Overview of the Quality System Regulation
Device History Record 820.184 & ISO 13485 § 7.5.1 (Executive Series #25)
Medical device regulation and the MHRA devices registration system
From the FDA Vault: A Shocking ExerciZe
Human Body Meets Medical Device: Are We Biocompatible?
Design Control for Medical Devices - Online introductory course
Is it time to re-evaluate your Design History File (DHF)?
Part 1: Medical Device Regulations
FDA Medical Device Regulation by Dr. Emily Zeitler (Dartmouth)
Device Master Record & Device History Record - A Regulatory
Medical Devices: Overview of US FDA regulatory process