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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.
Apply to manufacture Extemporaneous preparations, Autogenous vaccines, authorisations for Equine Stem Cell Centre (ESCCA) or Non-Food Animal Blood Bank (NFABBA).
Check what you need to do to sell cosmetic products in Great Britain.
How to register as a spring water producer, and the rules you must follow to produce and market spring water.
How to create a model of how your digital health product works and choose measures for your evaluation.
General advice on due diligence - electronic cigarettes devices and refill containers.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Find out the information you must give to customers on food products and how to give it.
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 know about and do to comply with the law and keep consumers safe.
How a marketing authorisation holder should report a defect with a veterinary medicine.
Guidance for manufacturers, importers and distributors.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Find out what information you need to show on products made of or containing meat that you sell to the public.
Check the tariff classification for flavour pods.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
Using an ecological momentary assessment to evaluate your digital health product.
Find out what compound products are, and how to import or move them from the EU to Great Britain.
Legal terms for veterinary medicines, marketing of non-medicinal products including medicinal words and phrases, how to complain.
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