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An action plan detailing how best practice can be shared across the NHS to improve the use of medicines and tackle medicines wastage.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
Guidance for healthcare professionals on using single-use medical devices.
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
UK guidance on re-manufacturing of Single-use medical devices.
Information for healthcare professionals on how pulse oximeters are regulated, home use and issues to look out for when using the devices
The Home Secretary has formally commissioned the Advisory Council on the Misuse of Drugs (ACMD) to conduct a longer-term review of cannabis-based products for medicinal use.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
This publication provides details of the code of practice that should be used for the responsible use of animal medicines on farms.
Details of the Yellow Card scheme, which is the system for recording adverse incidents with medicines and medical devices in the UK.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Safety leaflet on opioid medicines to help patients and their families reduce the risks of harm.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Check the veterinary product information database to find out if a medicine is safe to use on your pet or has been removed from sale
As a vet or pharmacist, you must follow legal requirements when working with controlled drugs in veterinary medicine.
How the MHRA makes decisions on what is a medicinal product (borderline products).
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