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A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
Strict global guidelines are available for use of expired primary health care drugs on the essential medicines list
Form for the testing of specified class A drugs on persons ages 18 or over.
Healthcare professionals prescribing montelukast should be alert to the risk of neuropsychiatric reactions in all patients including children and adolescents. Reported neuropsychiatric reactions include sleep disorders, hallucinations, anxiety and depression, as well as changes in behaviour and mood. Healthcare professionals...
Systemic fluoroquinolones must now only be prescribed when other commonly recommended antibiotics are inappropriate. This follows a review by the MHRA which looked at the effectiveness of current measures to reduce the identified risk of disabling and potentially long-lasting or...
How to contact MHRA for specific services or enquiries.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Guidance on medicines for food and non-food horses and record keeping requirements including the horse passport.
Legal requirements and good practice guidance for SQP retailers’ premises inspections.
Guide to the services offered by the mycology reference laboratory (MRL) to help medical professionals manage fungal infections.
Guidance on how to reclassify your medicine and how to name medicines.
This series brings together all documents relating to drug testing on arrest.
How to make sure an application relating to an authorisation for a veterinary medicine is complete and will pass validation.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
List of Field Safety Notices from 20 to 24 May 2024.
Information on clinical trials for medicines, how to apply for authorisation in the UK, how to manage your authorisation, reporting safety issues and details about the MHRA phase I accreditation scheme.
Scope of the review of the evidence for dependence on, and withdrawal from, prescribed medicines.
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