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GUIDELINE ON SUBMISSION OF DOCUMENTATION FOR REGISTRATION OF A MULTISOURCE (GENERIC) FINISHED PHARMACEUTICAL PRODUCT (FPP): QUALITY PART IN THE COMMON TECHNICAL DOCUMENT (CTD) FORMAT

Medicines Control Authority of Zimbabwe (MCAZ) (2012) C2
Source:
https://www.rrfa.co.za/wp-content/uploads/2012/11/CTD-guidelines-March-2013.pdf
Topics:
registration of drugs product registration registration and regulation of medicines medicine registration Licensed pharmaceutical products documentation National Guidelines country guidelines Zimbabwe medicines drugs
Countries:
Zimbabwe