Transcription of Dregs Couverture der - WHO
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HEALTHCARE TECHNOLOGY LIFE CYCLE medical DEVICE. Marketing Transfer Distribution Manufacture Testing Development Research PROVISION. regulations . Assessment of needs Global overview and Technology assessment Evaluation Planning De-commissioning guiding principles Maintenance Procurement Training Installation Operation ACQUISITION Commissioning UTILISATION. DEPARTMENT OF BLOOD SAFETY AND CLINICAL TECHNOLOGY. WORLD HEALTH ORGANIZATION. 1211 GENEVA 27 92 4 154618 2. SWITZERLAND. Fax 41 22 791 4836. E-mail WORLD HEALTH ORGANIZATION. GENEVA. medical DEVICE. regulations . Global overview and guiding principles WORLD HEALTH ORGANIZATION. GENEVA. WHO Library Cataloguing-in-Publication Data World Health Organization. medical device regulations : global overview and guiding principles. and supplies legislation and supplies . standards making management control ISBN 92 4 154618 2 (NLM Classification: WA 26). Acknowledgements This guide was prepared under the principal authorship of Dr Michael Cheng.
iv MEDICAL DEVICE REGULATIONS 6.2 Establishing basic regulatory programmes 25 6.2.1 Basic legislation 25 6.2.2 Sharing problem reports 25 6.3 Drafting a comprehensive policy or guideline on medical device
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