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Guidance on the collection, verification, and reporting of safety events in clinical trials of an investigational medicinal product.
How marketing authorisation holders should inform MHRA of a signal or an ADR to a medicine.
Information on how to report a serious undesirable effect (SUE) or safeguarding issue for cosmetic products.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Explanation for animal owners and veterinary health professionals on how the VMD calculates adverse event incidence rates for veterinary medicines
Non-arteritic anterior ischemic optic neuropathy (NAION), a condition that can cause sudden deterioration in vision, usually in one eye at a time, has been very rarely reported in association with semaglutide in the treatment of type 2 diabetes, weight management...
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Find out about the symptoms of COVID-19, what to do if you or your child has them and when to get medical help.
Overtime law - what is overtime, overtime pay, employee rights, part-time workers and time off in lieu
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