The life sciences industry represents one of the dominant economic sectors in the UK. Given the complexity of the European Regulatory Framework relating to the supply of human medicinal products this book gives an authoritative overview of the law as it currently stands.
This practical guide will address the regulatory procedures and day to day challenges for the authorisation and use of human medicinal products in the EU’s most regulated industry.
User-friendly, practical and pragmatic this book will prove an invaluable source of information for those who work in industry, regulatory authorities and for all persons who need to familiarise themselves with the relevant legislation in this fast moving industry sector.
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