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Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
UK guideline on GMP for decentralised manufacturing, ensuring compliance with EU GMP principles for safe, quality medicinal products.
Guidance on using the GEFS, which allows 30-day support attestations that cover an entire group of products for export.
The gender innovation policy initiative for Ethiopia conducted phone survey on a sample of 323 recently hired female factory workers
The Environment Agency’s Generic Design Assessment (GDA) of new nuclear power station designs and how we engage with others during the process.
The DCMS 5G Programme Industrial 5G Testbeds & Trials grant funding competition has now closed for applications. Officials are currently reviewing proposals.
Guidance for clinical trials that use Decentralised Manufactured Investigational Medicinal Products (IMPs).
Documents about the Generic Design Assessment (GDA) of Hitachi GE's UK Advanced Boiling Water Reactor (ABWR) new nuclear power station design.
MHRA’s mechanism for evaluating the justifications supplied by applicant organisations who plan to utilise decentralised manufacture.
Information on the new regulations for decentralised manufacture, including point of care and modular manufacture, which come into effect 23 July 2025.
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