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Find out which radioactive sources you need a licence to export and how to apply for one.
The information clients, principal designers, principal contractors and accountable persons need to keep.
Requirements for sponsor representatives using EHR (electronic health records) in clinical trials.
Guidance for Applicants wishing to apply for a Promising Innovative Medicines designation, pre-submission meeting or an EAMS Scientific Opinion.
Details of how Marketing Authorisation Holders can provide information on planned or potential future submissions, to the MHRA.
The guide, toolkit and further information for GB authorities with responsibility for consumer product safety.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
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