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Read about talking therapies and counselling for mental health problems.
Details the government's response to parts 1 and 2 of Dame Carol Black's independent review of drugs.
This series brings together all documents relating to drugs licensing.
The penalties if you are caught taking or dealing drugs - drug classification, fines and prison sentences
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Offenders with drug and alcohol problems are being put back on the straight and narrow through a new US-inspired sentencing approach to cut reoffending.
It's illegal to drive if you're unfit to do so because you're on legal or illegal drugs, or you have certain levels of drugs or medicine in your blood
Information for British nationals who are victims of rape and sexual assault in Tonga.
How the MHRA makes decisions on what is a medicinal product (borderline products).
The CAT has unanimously upheld the level of penalty imposed by the CMA for a market sharing agreement relating to 20mg hydrocortisone tablets.
Foresight project looking at how future scientific advances may affect our understanding of addiction and drug use.
Report a problem ('adverse incident') with a medical device or medicine to MHRA using the Yellow Card Scheme
When entering the UK, you need to prove your medicine is prescribed to you if it contains a controlled drug - find out what proof you need to get.
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)’
Guidance for veterinary medicines manufacturers and wholesale dealers in GB on selling and supplying products placed on the EU and UK markets before 1 January 2021 and the evidence you may need to provide.
Information for wholesale dealer licence holders about the medicines put on the UK market for UK patients that they cannot export or hoard.
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
How to prepare for implementation and compliance of the Safety Features Regulation.
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