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Guidance for the pharmaceutical industry on who can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
Data protection rules for businesses in recruiting staff, keeping staff records and using CCTV
Submission dates and how the submissions using the EC decision reliance procedure work.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
Find out the basic rules of VAT, how they apply to clubs and associations, and how to treat VAT on subscriptions and other payments.
How to market forest reproductive material (FRM) for forestry purposes, including regulations, registration, master certificates and licences.
Find out what a charity is, how VAT affects charities, how to treat a charity's income for VAT and what VAT reliefs a charity can get on what it buys.
Find out how to account for VAT on entertainment provided by your business.
Upper Tribunal Administrative Appeals Chamber decision by Judge Wikeley on 22 April 2024.
This toolkit is for Innovation Passport holders following the Innovative Licensing and Access Pathway (ILAP) and provides activities to support the design and development of medicines.
The government's summary of amendments to EU legislation concerning marketing standards for the fruit and vegetables sector.
Marking, labelling and marketing standards you must follow to import and export plant seeds, food and manufactured goods.
Guidance for the pharmaceutical industry on how to apply for an authorisation to place a veterinary medicine on the UK market or part of, or to expire one.
How to apply for marketing authorisation via this new procedure.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
The Lambert toolkit is for universities and companies that wish to undertake collaborative research projects with each other.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
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