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Register to vote Register by 18 June to vote in the General Election on 4 July.
Information for companies on the import and export of controlled drugs to and from the UK.
Reported problems with the supply of an animal medicine and the date when the issue is expected to be resolved.
Legal requirements and good practice guidance for SQP retailers’ premises inspections.
Information and guidance on a range of medical devices for users and patients.
Decisions made by the MHRA following investigations into complaints about advertising for licensed medicines.
How UK citizens or residents can get healthcare when visiting countries or territories outside the EU where the UK has reciprocal healthcare agreements.
The Commission on Human Medicines (CHM) advises ministers on the safety, efficacy and quality of medicinal products. CHM is an advisory non-departmental public body, sponsored by the Department of Health and Social Care .
Over two million doses of illegally traded medicines valued at almost £5m seized so far this year.
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...
Information and documents on Public Health England’s review of the evidence for dependence on, and withdrawal from, prescribed medicines.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
What you need to do to supply authorised medicines from Great Britain to Northern Ireland.
Placing a veterinary medicine on the market, including non-medicinal products, medicinal words and phrases, how to obtain advice, report non-compliance.
Project Orbis is a programme to review and approve promising cancer drugs helping patients access treatments faster.
How investigators and sponsors should manage clinical trials during COVID-19
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices.
Industry must notify the MHRA if they will not be using these flexibilities
The review of the safety of isotretinoin has concluded.
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