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VICH consultation until 31 July 2024 on guidelines relating to the technical requirements for demonstrating the safety of residues of veterinary drugs in food.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
How to use routinely collected data to evaluate your digital health product.
Lists of standards that businesses can use to show their products, services or processes comply with essential requirements of legislation.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Information about the Seafood Disruption Support Scheme.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to use a patient-reported outcomes and experiences study to evaluate your digital health product.
This guide sets out who has to apply for a permit, how to apply and explains the other rules covering travel to Antarctica.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
This guidance relates to the legal criteria for determining whether a building is considered a higher-risk building under the Building Safety Act 2022 and the Higher-Risk Buildings (Descriptions and Supplementary Provisions) Regulations 2023. It relates to the definition of higher-risk...
The generic Disposal System Safety Case demonstrates how a geological disposal facility can be designed, constructed and operated safely.
95% of people who voted in person in May's election found the process easy, research published today shows.
Guidance for manufacturers, importers and distributors.
How to use a crossover randomised controlled trial to evaluate your digital health product.
Introducing 3 innovative programmes to improve resilience to flooding and coastal change.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Contractual exit plans must be developed as an alternative to extension or evidence provided for why an extension is both legally allowed and value for money
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
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