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Pharmacovigilance system requirements
Sets out special provisions for Crown development for dealing with security-sensitive information in planning applications.
Guidance for non-UK qualified officers on how to apply for, or revalidate a Flag State Endorsement to work on UK-registered commercial vessels.
Apply for a High Potential Individual (HPI) visa if you've been awarded a qualification by an eligible university in the last 5 years - eligibility, fees, documents, switch, bring your partner and children
Who in the pharmaceutical industry can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
Tech Minister Saqib Bhatti's speech to the National Cyber Security Centre's CyberUK 2024 conference in Birmingham.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Information on how to revalidate a UK CoC (and UK GMDSS at the same time).
UK visa sponsorship information for employers - requirements, certificates and licences for Workers and Temporary Workers.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Guide to submitting practitioner licence applications to the Administration of Radioactive Substances Advisory Committee (ARSAC).
We are the government’s centre of expertise for infrastructure and major projects. IPA works with the Cabinet Office and HM Treasury .
Authorisation decisions on the time-limited use of hazardous substances of very high concern under UK REACH.
Businesses can form a partnership with a local authority to provide advice other local regulators must respect.
Guidance for applying for a Deck CoC for Commercial and Private Yachts.
Apply for authorisation of premises for the retail supply of POM-VPS and NFA-VPS veterinary medicines by suitably qualified persons (SQPs).
Prescribing or supplying veterinary medicines including requirements for registration and inspection of premises.
A guide for trade associations and other organisations that help groups of businesses manage their regulatory activity as a co-ordinator.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
This guide gives a summary of what providers should expect and what they need to do as part of an Ofsted inspection.
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