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Guidance on the collection, verification, and reporting of safety events in clinical trials of an investigational medicinal product.
The AQuA Book is Government guidance about how to produce robust, fit for purpose analysis. It's for all analysts, analytical managers and commissioners.
Explains planning controls relating to the storage of hazardous substances in England and how to handle development proposals around hazardous establishments.
Guidance on labelling for medicinal products used in clinical trials.
Formerly part of M18, technical guidance for industrial plant operators (and their contractors) who monitor effluent discharges to water and sewer.
Information on comparator products used in studies supporting abridged marketing authorisation application.
Check the tariff classification for preparations put up for retail sale.
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