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Detailed guidance, regulations and rules
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Data, Freedom of Information releases and corporate reports
How marketing authorisation holders should inform MHRA of a signal or an ADR to a medicine.
Guidance for vets and beekeepers on importing bee medicines when a product authorised in the UK is not suitable or available.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Who you should contact if a pet or other animal or human has an unexpected reaction to a veterinary medicine or a problem with a microchip
When a material is waste, is a by-product or meets ‘end of waste’ status.
How we evaluated pre-exposure prophylactic (preventative) treatments for COVID-19.
Healthcare professionals should be vigilant for suspected adverse reactions and safety concerns associated with e-cigarettes and e-liquids, commonly known as vapes. Please report adverse reactions to the Yellow Card scheme and promote vigilance among patients.
How to use a cost effectiveness analysis to evaluate your digital health product.
Information about the risks of taking valproate medicines during pregnancy.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Ultrasound has been used in medical practice throughout the world for at least 50 years.
These reports explain our assessment of the scientific evidence used to lead to regulatory decisions on the safety of medicines or medicines classes.
Antipsychotic drugs available in the UK, their side effects and their effect on dementia patients.
Impact of parental conflict on local services, including education, health and social care, court systems, and drug and alcohol services.
The Medicines and Healthcare products Regulatory Agency (MHRA) has today (9 April 2024) approved the medicine fosdenopterin (Nulibry) to treat the genetic disease Molybdenum Cofactor Deficiency (MoCD) Type A
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