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A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How a marketing authorisation holder should report a defect with a veterinary medicine.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
The ETL (or Energy Technology Product List, ETPL) is a government list of energy-efficient plant and machinery.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
Add your product to the Energy Technology List - the list of energy saving products eligible for Enhanced Capital Allowance tax relief
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
Legal terms for veterinary medicines, marketing of non-medicinal products including medicinal words and phrases, how to complain.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Guidance for suppliers and dealers.
How UK organisations that supply or import packaging should comply with extended producer responsibility (EPR) for packaging.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
If the UKCA marking applies to products you manufacture or supply, you will have specific obligations and responsibilities for compliance, depending on your role.
What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
Resources to help anyone developing or running a digital health product to conduct an evaluation.
Find out what a composite food product is, and the rules you need to follow to export or move these products from Great Britain to the EU and Northern Ireland.
Information for manufacturers.
Why it's important to evaluate digital health products that have been developed rapidly and how to choose evaluation methods in these circumstances.
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