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Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
The information that schools must provide the Department for Education (DfE).
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
There are changes to the legislation on reference medicinal products (RMPs) used to support abridged marketing authorisation applications.
Information about how the MHRA regulates medical devices in Northern Ireland and what legislation applies to manufacturers and suppliers.
This explains the rules governing address for service for intellectual property rights in the UK.
How to apply for an authorisation to manufacture authorised veterinary medicines or medicines marketed under the Exemptions for small pet animals.
Guidance explaining the operational requirements for Inshore Vessel Monitoring Systems (I-VMS) under the fishing licence condition.
Guidance for manufacturers, importers and distributors.
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