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Register to vote Register by 18 June to vote in the General Election on 4 July.
How marketing authorisation holders should inform MHRA of a signal or an ADR to a medicine.
Information about the risks of taking valproate medicines during pregnancy.
How to comply with the requirements on promoting medicines to the public and to prescribers and suppliers of medicines.
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 apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How we evaluated pre-exposure prophylactic (preventative) treatments for COVID-19.
Fresenius Kabi Limited have informed the MHRA of a packaging error with specific batches of Sodium Chloride Intravenous Infusion 0.9% Freeflex and Freeflex PLUS.
You may need to tell DVLA if you have Tourette's syndrome - download the correct form if you need to let them know.
How to use a cost effectiveness analysis to evaluate your digital health product.
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
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Advice for medical professionals to follow when assessing drivers with psychiatric disorders.
You must tell DVLA if your attention deficit hyperactivity disorder (ADHD) affects your driving - download the correct form to let them know.
Antipsychotic drugs available in the UK, their side effects and their effect on dementia patients.
Ultrasound has been used in medical practice throughout the world for at least 50 years.
Impact of parental conflict on local services, including education, health and social care, court systems, and drug and alcohol services.
Information for public health professionals on immunisation.
These reports explain our assessment of the scientific evidence used to lead to regulatory decisions on the safety of medicines or medicines classes.
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