"Médicaments Droit Grande-Bretagne." . . "Pharmaceutical Preparations standards Europe Legislation." . . "Drug Compounding standards Great Britain Guideline." . . "Quality Control Europe Legislation." . . "Drug Industry standards." . . "drugs" . . "Pharmaceutical Preparations standards Great Britain Guideline." . . "Drug Industry Great Britain Guideline." . . "good manufacturing practice" . . "Pharmacie Droit Pays de l'Union européenne." . . "LAW Health." . . . . "Drug Industry Europe Guideline." . . "Drug Industry Europe Legislation." . . "Drug Compounding standards Europe Guideline." . . "regulations" . . "Pharmaceutical Preparations standards Europe Guideline." . . "Médicaments Droit Pays de l'Union européenne." . . "good distribution practice" . . "Drug Compounding standards Europe Legislation." . . "Drug Industry Great Britain Legislation." . . "Quality Control Europe Guideline." . . "Drug Compounding standards Great Britain Legislation." . . "Legislation, Drug Europe Guideline." . . "Pharmaceutical Preparations standards Great Britain Legislation." . . "Pharmacie Droit Grande-Bretagne." . . "Quality Control Great Britain Guideline." . . "Legislation, Drug Great Britain Guideline." . . "Orange guide" . . . . . . . . . . "Electronic books"@en . . "Rules and guidance for pharmaceutical manufacturers and distributors 2007"@en . "Rules and guidance for pharmaceutical manufacturers and distributors 2007" . . . . . . . . . . . . . "Offering guidance to manufacturers of pharmaceutical products, this text brings together the latest pharmaceutical regulations, directives and guidance on a number of key issues." . . . . . . . . . . . . "Since its first publication in 1971 this text, commonly known as the 'Orange Guide', has been an essential reference for all involved in the manufacture or distribution of medicines in Europe. Although much of the text is available elsewhere, the Orange Guide collates in one convenient and authoritative source European and UK guidance documents and information on legislation relating to the manufacture and distribution of medicines for human use. Compliance with Good Manufacturing Practice and Good Distribution Practice requirements is essential in the production and distribution of medicines."@en . . . . . . . . . . . . . . . . . . . . "Quality Control Great Britain Legislation." . .