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Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Urgent safety updates arising from pharmacovigilance data, including reported adverse events, for veterinary medicines authorised in the UK.
Guidance on managing and using bed rails safely.
How investigators and sponsors should manage clinical trials during COVID-19
Organisational definitions of terms concerned with risk and risk-related matters.
Information for public health professionals on immunisation.
Advises on how planning can manage potential noise impacts in new development.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
The MHRA has reviewed the latest evidence relating to the very rare risk of PRES and RCVS associated with medicines containing pseudoephedrine
Provides clarity on the need for sustainability appraisal and strategic environmental assessment in relation to plan development.
Topical steroid products are safe and highly effective treatments for the management of a wide range of inflammatory skin diseases but have important risks, especially with prolonged use at high potency. In the coming months, as a result of regulatory...
When a material is waste, is a by-product or meets ‘end of waste’ status.
The review of the safety of isotretinoin has concluded.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
How marketing authorisation holders should inform MHRA of a signal or an ADR to a medicine.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
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