First Page | Document Content | |
---|---|---|
Health Pharmacology Pharmaceutical industry Pharmaceuticals policy Labels Federal Department of Home Affairs Swissmedic European Directorate for the Quality of Medicines Packaging and labeling Marketing authorization Tablet Dosage form | ZL000_00_021e_WL Guidance document Packaging for human medicinal products HMV4Add to Reading ListSource URL: www.swissmedic.chDownload Document from Source WebsiteFile Size: 594,33 KBShare Document on Facebook |
TIGes vet Q&A-update - Sept 2013DocID: 1rsZK - View Document | |
BPGWorksharingEMA-CMDvDocID: 1rr9m - View Document | |
CMDh meeting with representative of Interested Parties 19 May 2015 Type IA variation label implementation guidance.DocID: 1rqES - View Document | |
Annex VI: Implementation of mandatory VNeeS format for Veterinary regulatory submissions <> "Error*"Annex VI: Implementation of mandatory VNeeS format for Veterinary regulatory submissions \* MERGEFORMAT Annex VI: ImpleDocID: 1rqtS - View Document | |
Quasi Drug Rules in Japan December 2011 Quasi-drugs are a unique product classification in Japan. A quasi-drug is defined in Japan as products that have minimal to moderate pharmacologic activity but are restricted in usDocID: 1rpxR - View Document |