Tokyo, Japan
Uncategorized
IMDRF Presentation - Introduction of AHWP
IMDRF Presentation - Update on APEC LSIF RHSC
IMDRF Presentation - Update on China medical device regulatory
IMDRF Presentation - Medical Device Single Audit Program (MDSAP) Pilot Update
IMDRF Presentation - PAHO - Regulation of Medical Devices: a Regional approach
IMDRF Presentation - New Aspects in MD Regulations in the Russian Federation
IMDRF Presentation - Update on WHO work
IMDRF Presentation - Development of common terminology and code related to adverse event of medical device - NWI proposal sub committee report
IMDRF Presentation - DITTA contribution to IMDRF Stakeholder Forum
IMDRF Presentation - NWIP - Recognized Standards Phase II - PDF 12 March 2015
IMDRF Presentation - Regulatory update - ANVISA
IMDRF Presentation - Implementation of PMD Act - Japan Update
IMDRF Presentation - Update on EU regulatory developments
IMDRF Presentation - National Competent Authority Report Exchange Programme
IMDRF Presentation - Integrating Device Registries, UDI and Innovative Tools for Medical Device Evaluation
IMDRF Presentation - Regulated Products Working Group - Table of Contents Work Stream
IMDRF Presentation - RPS WG Update
IMDRF Presentation - Software as a Medical Device (SaMD) - Application of Quality Management System
IMDRF Presentation - Medical Device Single Audit Program (MDSAP) Working Group
IMDRF Presentation - Regulatory and Policy Updates - Health Canada
IMDRF Presentation - GMTA Collaboration with IMDRF: Third Anniversary
IMDRF Presentation - U.S. FDA Center for Devices and Radiological Health Update
Jurisdictional updates
Australian jurisdictional update