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Survivors can be ostracized from their communities, shunned by their families, denied justice and cut off from support networks. This can prevent community reconciliation and wider post-conflict stabilisation which is why the focus of the PSVI over the coming years...
The MHRA has authorised cabotegravir as 30 mg tablets and as a 600 mg long-acting injection administered every two months
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Information for patients, public and health care professionals.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
Guidance relating to blood clotting, myocarditis and Guillain-Barré Syndrome (GBS) after COVID-19 vaccination.
The Brucella Reference Unit (BRU) provides laboratory diagnostic and clinical management services for Brucella species.
How to spot Batrachochytrium salamandrivorans, what to do if you suspect it and measures to prevent its spread.
Details of certificates issued under the Special Import System for the top ten veterinary medicines that were imported 1 Oct - 31 Dec 2023.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices.
You may need to tell DVLA if you've had a transient ischaemic attack (TIA) - download the correct form if you need to let them know
Advice for health professionals on tick-borne encephalitis (TBE) including symptoms, diagnosis and epidemiology.
Details of certificates issued under the Special Import System for the top ten imported veterinary medicines 1 April - 30 June 2023.
The MHRA will introduce a patient alert card to increase awareness among men taking finasteride about potential psychiatric and sexual side effects
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.
Monitoring significant occupational exposures to HIV, hepatitis B and hepatitis C in healthcare workers, and advising on avoiding injuries.
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
UK Health Security Agency's laboratories provide a comprehensive range of microbiological tests and services.
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