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How to conform with the legal requirements for placing medical devices on the market.
Environmental regulations and guidance on offshore oil and gas exploration and production, offshore gas unloading and storage and offshore carbon dioxide storage activities
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Find out which regulations apply to your products and where to go for further information on how to comply with them.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
This guidance summarises the types of defects to which the leaseholder protections in the Building Safety Act 2022 apply.
A complete list of 5G projects involved in the 5G Testbeds and Trials Programme
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Answers to frequently asked questions on Approved Document S, which sets standards for installation of electric vehicle charge points or cable routes.
Guidance for manufacturers, importers and distributors.
Information for patients, public and health care professionals.
This series brings together documents relating to Home Office research and evaluation on migration.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to use a cost utility analysis to evaluate your digital health product.
The Intellectual Property Office offers different methods of accelerating the processing of your patent application.
The UK Good Laboratory Practice Monitoring Authority (UK GLPMA) recognises that there are potential challenges COVID-19 will present to members of the GLP monitoring programme.
Find out if you need to use the UKCA (UK Conformity Assessed) marking on products you manufacture or handle.
Actions companies need to take to export nuclear-related items.
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