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How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Advice for manufacturers of Class I medical devices for placing products on the UK market
Claim relief on import duty and VAT when importing miscellaneous documents and related articles into the UK.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Find out if you will need to use the new UKNI marking and how to use it.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Find out if you need to use the UKCA (UK Conformity Assessed) marking on products you manufacture or handle.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Guidance on Animal Test Certificates (ATCs) required to carry out the field trial of a veterinary medicine in animals (clinical trial) in the UK.
Lists of standards that businesses can use to show their products, services or processes comply with essential requirements of legislation.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Check the regulations on aircraft parts imported with a certificate of airworthiness.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
Legal terms for veterinary medicines, marketing of non-medicinal products including medicinal words and phrases, how to complain.
To help you protect, manage and enforce your intellectual property (IP) rights in Laos.
Advice on writing clear notices and maximising replies to your FSNs.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
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