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Export controls applying to Weapons of Mass Destruction (WMD) related activities – transfer of technology and provision of technical support
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
Find out about the Industry Security Assurance Centre (ISAC) and its associated responsibilities.
What to do if you have an electronic tag (including curfew tags, location tags and alcohol tags) and how to contact the Electronic Monitoring Service (EMS).
Guidance for organisations involved in any aspect of the pharmaceutical lifecycle or GLP studies regulated by MHRA, covering the approval of paper documents when working from home
British travellers to the US must register with the Electronic System for Travel Authorisation (ESTA) before their journey
Since, April 2024, the MHRA has been using Lorenz DocuBridge for eCTD management in product licence submissions. This change is part of the modernisation of the MHRA’s Legacy Systems and is one of the initial tools launched in the RegulatoryConnect...
How to show the MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
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