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Apply for an Academic Technology Approval Scheme (ATAS) certificate, to study certain subjects in the UK.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
How an innovative funding mechanism is saving lives by speeding up the availability of vaccines and making them affordable.
Check the tariff classification for components in sets for dental repair.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
The review of the safety of isotretinoin has concluded.
Check the tariff classification for antimicrobial bathing systems.
Apply for a promising innovative medicine (PIM) designation or scientific opinion for your medicine from MHRA.
You must tell DVLA if you suffer from ankylosing spondylitis and it affects your ability to drive safely - download the correct form to let them know
We give statutory advice to ministers on the risks to human health and the environment from the release of genetically modified organisms (GMOs). ACRE is an advisory non-departmental public body, sponsored by the Department for Environment, Food & Rural Affairs...
These reports explain our assessment of the scientific evidence used to lead to regulatory decisions on the safety of medicines or medicines classes.
Claim relief on import duty and VAT when importing miscellaneous documents and related articles into the UK.
Check the tariff classification for low shoes.
We help people, businesses and the UK economy by promoting competitive markets and tackling unfair behaviour. CMA is a non-ministerial department.
Information for applicants in England about the outcome of the national Clinical Impact Awards (NCIAs) 2023 and the appeals process.
Apply for a higher education course, track your application and accept or reject your offers.
This series brings together all documents relating to Allied Joint Publication (AJP).
Check timescales for the Legal Aid Agency (LAA) to process your work (eg prior authority application, graduated fee claims).
The MHRA is part of the Access Consortium along with the Therapeutic Goods Administration, Health Canada, Health Sciences Authority of Singapore and Swissmedic.
An overview of the future requirements for rapid COVID-19 diagnostic assays for antigen lateral flow devices.
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