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Information for patients, healthcare professionals and developers of new medicines
How traditional herbal medicines and homeopathic medicines will be treated by the MHRA.
How to prepare for implementation and compliance of the Safety Features Regulation.
How to package medicines for sale and what information you must provide to consumers and healthcare professionals.
How veterinary medicines can be advertised.
How to apply for, update and cancel licences for the manufacture, import and wholesale of human and veterinary medicines.
What you need to do to supply authorised medicines from Great Britain to Northern Ireland.
Legal terms for veterinary medicines, marketing of non-medicinal products including medicinal words and phrases, how to complain.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
The Medicines and Healthcare products Regulatory Agency regulates medicines, medical devices and blood components for transfusion in the UK. MHRA is an executive agency, sponsored by the Department of Health and Social Care .
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
How to comply with the exemption from the Veterinary Medicines Regulations that allow certain animal medicines to be sold without an authorisation.
How to get a parallel import licence for your medicine in the UK, including pharmacovigilance requirements and submitting your application.
Get help to classify organic chemicals that contain certain permitted additives or can be dissolved in water, for import and export.
Links to EU guidance, as it stood immediately before end of transition period.
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