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A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Get help to classify edible vegetables, roots, tubers, herbs, spices, fruit, nuts and peel for import and export.
The MHRA is continuing to accept Active Substance Master Files (ASMFs) and Certificates of Suitability (CEPs)
How to submit your periodic safety update report report (PSUR) or periodic benefit risk evaluation report (PBRER)
How to apply for, update and cancel licences for the manufacture, import and wholesale of human and veterinary medicines.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Get help to classify organic chemicals that contain certain permitted additives or can be dissolved in water, for import and export.
Reported problems with the supply of an animal medicine and the date when the issue is expected to be resolved.
Details of the Yellow Card scheme, which is the system for recording adverse incidents with medicines and medical devices in the UK.
Apply for an import certificate to import a medicinal product into the UK for veterinary use.
Guidance on medicines for food and non-food horses and record keeping requirements including the horse passport.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Information for patients, healthcare professionals and developers of new medicines
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