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What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
These reports explain our assessment of the scientific evidence used to lead to regulatory decisions on the safety of medicines or medicines classes.
You must get permission to export certain drugs and medicines.
Information about new applications, post-licensing, advertising, product information and fees.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
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...
Advice for medical professionals to follow when assessing drivers with drug or alcohol misuse or dependence.
Apply for a promising innovative medicine (PIM) designation or scientific opinion for your medicine from MHRA.
How to submit your periodic safety update report report (PSUR) or periodic benefit risk evaluation report (PBRER)
How to register veterinary practice premises for veterinary surgeons to supply veterinary medicines.
How a manufacturer can apply for approval to supply a non-compliant medical device on humanitarian grounds.
Check what side effects people have reported when they've taken a medicine.
This guide is about infections that occur in people who inject drugs (PWID).
Register as a manufacturer, importer or distributor of active substances for use in veterinary medicines.
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 .
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
Information for companies on the import and export of controlled drugs to and from the UK.
What is considered off-label use of a medical device and examples of it.
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