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Register to vote Register by 18 June to vote in the General Election on 4 July.
Apply for your site to be approved to host heavy goods vehicle (HGV) or Driver Certificate of Professional Competence (CPC) part 4 tests.
Prescribing or supplying veterinary medicines including requirements for registration and inspection of premises.
Pharmacovigilance system requirements
What we check and how you apply for approval.
Apply for a licence that lets you import, move and keep normally prohibited material in England and Wales.
Professional Footballers’ Association trade union: annual returns, rules, statement to members, decisions and other related documents.
If your business sells amateur plant protection products (PPPs) in Great Britain, register to comply with regulations.
Find out what you need to do and what HMRC standards you must meet before registering as a professional tax agent.
How to apply for marketing authorisation via this new procedure.
Visit the UK as a Standard Visitor for tourism, business, study (courses up to 6 months), medical treatment and other activities. Find out whether you need a Standard Visitor visa, or can visit without a visa.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
The actions to take for sourcing medicines in different circumstances.
SIA regulation: how the SIA enforces the law and what the penalties are for breaking it.
Overview of professional regulation and registration, and annual report and accounts for 2021 to 2022.
To protect your patent outside of the UK, you usually need to apply in each country you want protection in.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
A course to help school leaders and headteachers develop the knowledge behind expert school leadership and apply it to become an outstanding headteacher.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Registers of authorised manufacturers, wholesale dealer sites and retailers.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
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