Name of Recipient F11 to next

First Page		Document Content
Date: 2013-10-09 09:37:44 Quality Research Good distribution practice Validation Health Qualified Person Medicine European Directive on Traditional Herbal Medicinal Products European Medicines Agency Pharmaceuticals policy Clinical research Pharmaceutical industry		Name of Recipient F11 to next Add to Reading List Source URL: ec.europa.eu Download Document from Source Website File Size: 362,72 KB Share Document on Facebook

	French National Agency for Medicines and Health Products Safety Certificate No: 2016/BPD/53 CERTIFICATE OF GDP COMPLIANCE OF A WHOLESALE DISTRIBUTOR D DocID: 1qNGU - View Document
	Be GDP Ready! A Good Distribution Practice Training & Workshop specially brought to you by SMF LifeSciences Industry Group COURSE DETAILS Dates: DocID: 1jnTo - View Document
	Guidelines on Good Distribution Practice of Medicinal Products for Human Use (94/CText with EEA relevance) Introduction These guidelines have been prepared in accordance with Article 10 of Council Directive 92/2 DocID: 1bk8O - View Document
	Current Global GMP Status and Trends With Focus on EU & PIC/S JPMA Annual Meeting, Tokyo & Osaka, September 2012 Dr.-Ing. Stephan Rönninger Pharma Medicines Technical Operations Global Quality & Compliance, F. Hoffmann- DocID: 17QHF - View Document
	ASMI Good Supplier Practice Guidelines – January[removed]Good Supplier Practice AN INDUSTRY GUIDELINE For the management of quality starting and packaging materials DocID: Wm70 - View Document