EU Medical Device Regulation 2017-745 4 Part 58 - Good Laboratory

Name: EU Medical Device Regulation 2017-745 4 Part 58 - Good Laboratory
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Description

Part 58 - Good Laboratory Practice

Part 11 - Scope & Application August 2003

as described within ICH Q14 Analytical Procedure Development

US FDA Title 21 CFR Parts

Hazard Analysis

EU Medical Device Regulation 2017-745 4 Part 58 - Good LaboratoryEU Medical Device Regulation 2017 745 REGULATION (EU) 2017 745 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 5 April 2017 on medical devices, amending Directive 2001 83 EC, Regulation (EC) No 178 2002 and Regulation (EC) No 1223 2009 and repealing Council Directives 90 385 EEC and 93 42 EEC

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