<--- Back to Details
First PageDocument Content
Medical technology / Global Harmonization Task Force / Medical device / CE mark / Unique Device Identification / Notified Body / Medical equipment / Medicine / Technology
Date: 2013-10-03 12:39:14
Medical technology
Global Harmonization Task Force
Medical device
CE mark
Unique Device Identification
Notified Body
Medical equipment
Medicine
Technology

Microsoft Word - Recast_NAM.doc

Add to Reading List

Source URL: ec.europa.eu

Download Document from Source Website

File Size: 43,06 KB

Share Document on Facebook

Similar Documents

Medical equipment / Medicine / Health / Global Harmonization Task Force / Food and Drug Administration / Technology / Medical device / Health Canada

IMDRF Presentation - NCAR update

DocID: 1rjHy - View Document

Medicine / Medical equipment / Medical technology / Health / Technology / ISO 13485 / Notified Body / Global Harmonization Task Force / CE marking / Medical device / Medsafe / Medicines and Healthcare products Regulatory Agency

White Paper Proposal for a New Zealand Regulatory Scheme for Medical Devices

DocID: 1qbuf - View Document

Medical equipment / Clinical research / Healthcare quality / Global Harmonization Task Force / Drug safety / Pharmaceuticals policy / Pharmacovigilance / Vigilance / Adverse event / Asia-Pacific Economic Cooperation / Medical device

IMDRF Presentation: Update from APEC LSIF RHSC

DocID: 1pHIm - View Document

Medical equipment / Global Harmonization Task Force / National Center for Atmospheric Research

IMDRF Presentation: IMDRF National Competent Authority Report (NCAR) exchange program

DocID: 1pzyV - View Document

Medical equipment / Global Harmonization Task Force / Medical device / Food and Drug Administration

IMDRF Presentation: National Competent Authority Report Exchange Programme

DocID: 1pjXG - View Document