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Get information on teacher training courses, funding, pay scales and how to make a great application
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Pharmacovigilance system requirements
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Check how much your visa application costs in the country you’re in
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Look up a trade mark to see if something identical or similar to your brand is already registered.
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.
You must tell DVLA if you have a brain abscess, cyst or encephalitis - download the correct form to let them know
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
You must register and declare ozone-depleting substances (ODS) for laboratory or analytical uses.
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
Short-term study visa - prepare supporting documents, apply, book and attend an appointment, what happens at the UK border
The diagnosis, management and epidemiology of Bacillus spp.
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
Student visa - check which courses you can study, prepare supporting documents, apply, what happens at the UK border
Check the tariff classification for flavour pods.
Use the rolling review route when you want to submit your eCTD dossier in separate parts for pre-assessment instead of making a full consolidated document submission.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
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