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Pharmacovigilance system requirements
Check the regulations on aircraft parts imported with a certificate of airworthiness.
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.
Check how much your visa application costs in the country you’re in
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
Form to report patients meeting the case definition.
Guidance and information about high consequence infectious diseases and their management in England.
Look up a trade mark to see if something identical or similar to your brand is already registered.
How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
You must tell DVLA if you have a brain abscess, cyst or encephalitis - download the correct form to let them know
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
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.
Find out who can get a free rapid lateral flow test, how to use the test and what your test result means.
Advice for medical professionals to follow when assessing drivers with neurological disorders.
Student visa - check which courses you can study, prepare supporting documents, apply, what happens at the UK border
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.
The MHRA is part of the Access Consortium along with the Therapeutic Goods Administration, Health Canada, Health Sciences Authority of Singapore and Swissmedic.
Use an OGEL to export controlled dual-use or military goods, software and technology overseas.
Details of certificates issued under the Special Import System for the top ten veterinary medicines that were imported 1 Oct - 31 Dec 2023.
These temporary good manufacturing practice (GMP) flexibilities will be allowed to address the current exceptional circumstances
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