EUROPEAN COMMISSION DIRECTORATE GENERAL for HEALTH and CONSUMERS Consumer Affairs Health technology and Cosmetics MEDDEV[removed]rev2

First Page		Document Content
Date: 2013-10-03 11:56:15 Health Medical technology Global Harmonization Task Force Pharmaceuticals policy Medical device Food and Drug Administration Medical Devices Directive CE mark Regulatory requirement Medicine Technology Medical equipment		EUROPEAN COMMISSION DIRECTORATE GENERAL for HEALTH and CONSUMERS Consumer Affairs Health technology and Cosmetics MEDDEV[removed]rev2 Add to Reading List Source URL: ec.europa.eu Download Document from Source Website File Size: 221,00 KB Share Document on Facebook

	IMDRF Presentation - NCAR update DocID: 1rjHy - View Document
	White Paper Proposal for a New Zealand Regulatory Scheme for Medical Devices DocID: 1qbuf - View Document
	IMDRF Presentation: Update from APEC LSIF RHSC DocID: 1pHIm - View Document
	IMDRF Presentation: IMDRF National Competent Authority Report (NCAR) exchange program DocID: 1pzyV - View Document
	IMDRF Presentation: National Competent Authority Report Exchange Programme DocID: 1pjXG - View Document