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Get information on teacher training courses, funding, pay scales and how to make a great application
Get endorsement for the Global Talent visa to work in the UK as a researcher or academic leader - fellowship, UKRI endorsement, peer review.
Pharmacovigilance system requirements
Check how quickly you’ll receive a decision on your UK visa application if you are applying from outside the UK.
Applications received to amend the specification of a patent under sections 27 and 75 before the court and the Office.
Actions that trial sponsors should consider to build resilience into clinical trial design
Information about the EU Regulations and their implementation in Northern Ireland
Check how much your visa application costs in the country you’re in
Apply for a Temporary Work - Religious Worker visa to do religious work in the UK - getting sponsored, fees, eligibility, family members
Guidance for UK companies on winning business from international aid and development projects.
Protocols and procedures for testing the distinctiveness, uniformity and stability (DUS) of certain agricultural and vegetable plants.
How to object to the registration of a lasting or enduring power of attorney - including forms and fees
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
The UK Good Laboratory Practice Monitoring Authority (UK GLPMA) recognises that there are potential challenges COVID-19 will present to members of the GLP monitoring programme.
Apply for a Minister of Religion visa (T2) if you've been offered a job in a faith community - eligibility, extend or switch, knowledge of English, bring your family
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
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.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
Guidance for organisations involved in any aspect of the pharmaceutical lifecycle or GLP studies regulated by MHRA, covering the approval of paper documents when working from home
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