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Guidance for industry on flexible approaches we are taking on good distribution practices.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
This guidance demonstrates stakeholders, including the government, working together to address supply issues.
Qualified Persons (QPs) should follow the below guidance on the flexible approaches we are taking for medicines imported from third countries.
How to prepare for implementation and compliance of the Safety Features Regulation.
These temporary good manufacturing practice (GMP) flexibilities will be allowed to address the current exceptional circumstances
Applications closed open for the 2018 Nuclear Decommissioning Authority (NDA) Estate Supply Chain Awards on 5 September.
List of manufacturers and their medical devices granted an exemption by MHRA. The list also includes manufacturers whose exemption expired or was cancelled.
We have more than 10 years’ experience of successfully working with our customers to develop solutions across the radioactive waste lifecycle and provide access to the full range of treatment, logistics, and disposal techniques and technology in the UK, Europe,...
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