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How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
How the protected online filing (PROOF) scheme can help you prevent fraudulent changes to your company.
As a vet or pharmacist, you must follow legal requirements when working with controlled drugs in veterinary medicine.
When entering the UK, you need to prove your medicine is prescribed to you if it contains a controlled drug - find out what proof you need to get.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
Licence and registration application information for companies that deal in precursor chemicals.
Prove the origin of your goods if you’re trading with a country that has a trade agreement with the UK, or is covered by the Developing Countries Trading Scheme.
Find out about the registered dealers in controlled oil (RDCO) scheme.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
How to use the simplified declaration procedure when importing goods into the UK.
Sections (100.01 - 100.06) last updated October 2021.
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How UK private maritime security companies (PMSCs) get sealed and signed physical certificates to meet documentation requirements of overseas governments.
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