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Placing a veterinary medicine on the market, including non-medicinal products, medicinal words and phrases, how to obtain advice, report non-compliance.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
If you're advertising or marketing, including direct marketing, you must be accurate and honest and follow the advertising codes of practice
All marketing and advertising must be: an accurate description of the…
Advertising to consumers The Consumer Protection from Unfair Trading…
There are 2 advertising codes of practice that describe how businesses…
You must describe your product accurately. This means if you make a claim…
You must check if customers want to be contacted by fax, phone, post or…
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
Quality and labelling rules for growing, packing, distributing, importing and selling fresh fruit and vegetables.
How the MHRA processes variations to Marketing Authorisations (MAs)
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Steps to help grow your business - finding finance, mentors, increasing sales and developing products and services
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Submission dates and how the submissions using the EC decision reliance procedure work.
Who in the pharmaceutical industry can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
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.
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
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