Transcription of Dregs Couverture der - WHO
{{id}} {{{paragraph}}}
Example: barber
Dregs Couverture der - WHO
MEDICAL DEVICEREGULATIONSG lobal overview andguiding principlesWORLD health ORGANIZATIONGENEVADEPARTMENT OF BLOOD SAFETY AND CLINICAL TECHNOLOGYWORLD health ORGANIZATION1211 GENEVA 27 SWITZERLANDFax41 22 791 4836E-mail 4 154618 2 HEALTHCARE TECHNOLOGY LIFE CYCLEDe-commissioningMaintenanceTraining OperationTechnology assessmentEvaluationPlanningProcurementI nstallationCommissioningAssessment of needsResearchDevelopmentTestingManufactu reMarketingTransferDistributionACQUISITI ONUTILISATIONPROVISIONMEDICAL DEVICEREGULATIONSG lobal overview andguiding principlesWORLD health ORGANIZATIONGENEVAA cknowledgementsThis guide was prepared under the principal authorship of Dr Michael Cheng. It is basedon a similar publication issued by the Pan American health organization (PAHO) in1999 that reviewed the Canadian Medical Devices Regulatory comments and suggestions made by members of the Global Harmonization TaskForce and those of many other reviewers are gratefully department of Blood Safety and Clinical Technology thanks the Governments ofItaly and Luxembourg for their continued support to its
DEPARTMENT OF BLOOD SAFETY AND CLINICAL TECHNOLOGY WORLD HEALTH ORGANIZATION 1211–GENEVA–27 ... standards 3.Policy making 4.Risk management 5.Quality control I.Title. ISBN 92 4 154618 2 (NLM Classification: WA 26) Contents iii Foreword v ... may have production facilities that will require good manufacturing practice and complex
Loading..
Tags:
Information
Domain:
Source:
Link to this page:
Please notify us if you found a problem with this document: