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Project Orbis is a programme to review and approve promising cancer drugs helping patients access treatments faster.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Fifteen additional synthetic opioids are now under the strictest controls to prevent drug related deaths and ensure anyone caught supplying them faces tough penalties.
Information about the DCIA programme, with guidance on how to participate in the Pilot competition
An overview of government's programme to develop and manufacture new medicines, digital health products and medical technologies.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
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.
The Advisory Council on the Misuse of Drugs makes recommendations to government on the control of dangerous or otherwise harmful drugs, including classification and scheduling under the Misuse of Drugs Act 1971 and its regulations. ACMD is an advisory non-departmental...
We help people, businesses and the UK economy by promoting competitive markets and tackling unfair behaviour. CMA is a non-ministerial department.
This guide provides information about being arrested in Turkey and what conditions are like in prison there.
Information for patients, healthcare professionals and developers of new medicines
The review will examine the harm that drugs cause and look at prevention, treatment and recovery.
The penalties if you are caught taking or dealing drugs - drug classification, fines and prison sentences
FCDO travel advice for USA. Includes safety and security, insurance, entry requirements and legal differences.
New measures will mean EV owners benefit from easier and more convenient access to chargepoints.
This series brings together all documents relating to drugs licensing.
Support for MedAccess will be used to negotiate lower prices for vital malaria drugs and diagnostic tests for people in countries affected by the disease.
How marketing authorisation holders should inform MHRA of a signal or an ADR to a medicine.
Summarises progress made and outlines further critical steps required to ensure that the right drugs are available
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