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How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Design, build and operate APIs in a consistent way
Volume 19 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
How to use the calculators to work out a nutrient budget for residential developments in nutrient neutrality catchments.
Find out about the verification checks and what to expect during a visit if you have applied for verification and paid your fee for the Scheme.
Advice for medical professionals to use when assessing drivers with cardiovascular disorders.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Explanations of the different terms you might see on your driving licence
Joint statement between UK and Australia, following the tenth Australia-UK Ministerial Meeting (AUKMIN) held in Edinburgh on 20 July 2018.
Find out if you need to use the UKCA (UK Conformity Assessed) marking on products you manufacture or handle.
AMRHAI (antimicrobial resistance and healthcare associated infections) is the national reference unit for investigating AMR in healthcare-associated bacteria.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Two new mascots are helping bring to life the history and wildlife of a city centre urban watercourse.
How to conform with the legal requirements for placing medical devices on the market.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
BAT for diesel engines on an installation that are classed as new medium combustion plant, operating up to 500 hours a year that are exempt from emission limit values (ELVs).
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
How to renew marketing authorisations for products granted through different routes and at different times.
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