PICS GUIDE FOR GMP › PIC/S Guide to Good Manufacturing Practice for Medicinal Products
Included in this current edition are the following subparts:
2015 EDITION - Oct. 1, 2015
2017 ANNEXES - Jan. 1, 2017
2017 ANNEXES - Jan. 1, 2017
Customers who bought this document also bought:
BS-EN-ISO-13485Medical devices. Quality management systems. Requirements for regulatory purposes
SOR/98-282
Medical Devices Regulations (Canada)
BS-EN-ISO-15223-1
Medical devices. Symbols to be used with information to be supplied by the manufacturer
Document Number
PE-009-12
Revision Level
2015 EDITION
Status
Current
Publication Date
Oct. 1, 2015