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Apply for an Academic Technology Approval Scheme (ATAS) certificate, to study certain subjects in the UK.
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.
Form to report patients meeting the case definition.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
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.
Check what you need to do to employ teachers who are non-UK citizens.
Look up a trade mark to see if something identical or similar to your brand is already registered.
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
Check how much your visa application costs in the country you’re in
Advice for medical professionals to follow when assessing drivers with neurological disorders.
Use an OGEL to export controlled dual-use or military goods, software and technology overseas.
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
How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
The MHRA is part of the Access Consortium along with the Therapeutic Goods Administration, Health Canada, Health Sciences Authority of Singapore and Swissmedic.
Student visa - check which courses you can study, prepare supporting documents, apply, what happens at the UK border
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
Information on how to gain a UK CoC for Engineering/Electro-Technical Officers or Engineering Watch Rating Certificate
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
Licences and authorisations to import genetic material, research and diagnostic samples, trade samples and display items, and some live animals and animal products.
Volume 23 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
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