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UK Guidance on Wholesale Distribution Practice

Aug 9, 2016 by admin in PHARMACY Comments Off on UK Guidance on Wholesale Distribution Practice

UK Guidance on Wholesale Distribution Practice The Application and Inspection Process “What to Expect” Applicants for a new wholesale dealer’s licence (WDA(H)) or existing licence holders wishing to vary their…

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UK Guidance on the Manufacture, Importation and Distribution of Active Substances

Aug 9, 2016 by admin in PHARMACY Comments Off on UK Guidance on the Manufacture, Importation and Distribution of Active Substances

UK Guidance on the Manufacture, Importation and Distribution of Active Substances Introduction EU Directive 2001/83/EC lays down the rules for the manufacture, import, marketing and supply of medicinal products and…

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MHRA: Licensing, Inspection and Enforcement for Human Medicines

Aug 9, 2016 by admin in PHARMACY Comments Off on MHRA: Licensing, Inspection and Enforcement for Human Medicines

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UK Legislation on Brokering Medicines

Aug 9, 2016 by admin in PHARMACY Comments Off on UK Legislation on Brokering Medicines

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UK Legislation on Wholesale Distribution

Aug 9, 2016 by admin in PHARMACY Comments Off on UK Legislation on Wholesale Distribution

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EU Legislation on Wholesale Distribution and Brokering Medicines

Aug 9, 2016 by admin in PHARMACY Comments Off on EU Legislation on Wholesale Distribution and Brokering Medicines

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UK Guidance on Brokering Medicines

Aug 9, 2016 by admin in PHARMACY Comments Off on UK Guidance on Brokering Medicines

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EU Legislation on Manufacture and Importation

Aug 9, 2016 by admin in PHARMACY Comments Off on EU Legislation on Manufacture and Importation

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UK Legislation on the Manufacture, Importation and Distribution of Active Substances

Aug 9, 2016 by admin in PHARMACY Comments Off on UK Legislation on the Manufacture, Importation and Distribution of Active Substances

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Guidelines on Good Distribution Practice of Medicinal Products for Human Use (2013/C 343/01)

Aug 9, 2016 by admin in PHARMACY Comments Off on Guidelines on Good Distribution Practice of Medicinal Products for Human Use (2013/C 343/01)

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