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A list of 10 criteria that represent good practice in creating, applying and enforcing design codes.
This guidance explains our competition process and how your proposal is assessed.
An overview of the future requirements for rapid COVID-19 diagnostic assays for antigen lateral flow devices.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
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