Description

Book Synopsis
The 2022 edition of the Rules and Guidance for Pharmaceutical Distributors, the 'Green Guide', is the essential reference for all distributors, brokers of human medicines, importers and distributors of active substances in the UK.It provides you with the single authoritative source of European good distribution practices and UK guidance, information and UK legislation on these activities.The new 5th edition has been updated to incorporate changes made after the UK's exit from the European Union on the 31st January 2020.It also incorporates new guidance on pharmacovigilance for wholesalers, the naming of sites on a licence, self-inspection, and the responsible person for import.It brings together EU guidance on good distribution practice and the MHRA's expectations for compliance. There is also a new flowchart for the registration of handling active substances

Rules and Guidance for Pharmaceutical

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£64.80

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RRP £72.00 – you save £7.20 (10%)

Order before 4pm today for delivery by Sat 20 Dec 2025.

A Paperback / softback by Medicines and Healthcare Products Regulatory Agency

15 in stock


    View other formats and editions of Rules and Guidance for Pharmaceutical by Medicines and Healthcare Products Regulatory Agency

    Publisher: Pharmaceutical Press
    Publication Date: 22/03/2022
    ISBN13: 9780857114419, 978-0857114419
    ISBN10: 0857114417
    Also in:
    Chemical, biotechnology and pharmaceutical Distribution and logistics management

    Description

    Book Synopsis
    The 2022 edition of the Rules and Guidance for Pharmaceutical Distributors, the 'Green Guide', is the essential reference for all distributors, brokers of human medicines, importers and distributors of active substances in the UK.It provides you with the single authoritative source of European good distribution practices and UK guidance, information and UK legislation on these activities.The new 5th edition has been updated to incorporate changes made after the UK's exit from the European Union on the 31st January 2020.It also incorporates new guidance on pharmacovigilance for wholesalers, the naming of sites on a licence, self-inspection, and the responsible person for import.It brings together EU guidance on good distribution practice and the MHRA's expectations for compliance. There is also a new flowchart for the registration of handling active substances

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