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MHRA Guidance: Applying for a Licence to Market a Medicine in the UK and Electronic Application Forms (eAF)
The UK Medicines and Healthcare products Regulatory Agency (MHRA) has provided guidance on applying for a licence to market a medicine in the UK and on using electronic Application Forms (eAFs) for medicines licensing applications. The first guidance explains the marketing authorisation application process, including electronic submissions, supporting documentation, product naming, fast-tracking, rejection, and fees. The second explains how applicants can download, complete,
Sharan Murugan
11 hours ago4 min read