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Register as a manufacturer, importer or distributor of active substances.
This is a work sharing model for the co-ordinated assessment of a generic application that has been filed with multiple Access Consortium agencies.
Guidance for UK wholesalers and manufacturers on how to import human medicines including unlicensed medicines, how to apply for a licence and how much it costs.
Find out about help you can get moving from benefits to work - work trials, programmes and clubs, New Enterprise Allowance, help with drug or alcohol problems, carer support
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Marketing Authorisation Holders should review their manufacturing processes to identify and, if found, to mitigate the risk of nitrosamine impurities being present.
New 10-year plan to expand and improve the drug and alcohol workforce published.
Get endorsement for the Global Talent visa to work in the UK as a researcher or academic leader - fellowship, UKRI endorsement, peer review.
An overview of the process including submitting or fast-tracking an application, naming your medicine and paying fees.
The New Active Substance Work Sharing Initiative (NASWSI) has successfully approved several medicines through this international collaboration and continues to foster cooperation and strong relationships between its Access partners. The Biosimilar Work Sharing Initiative (BSWSI) builds on this success.
Senior Efficacy Assessor vacancies, working in the regulation of veterinary medicines.
Two pharmacists who sold ‘industrial’ quantities of Class C controlled drugs were yesterday sentenced to two years’ imprisonment each, suspended for 24 months, at Southwark Crown Court following an investigation by the Criminal Enforcement Unit of the Medicines and Healthcare...
How we engage and involve patients and the public in our regulatory decision-making.
Apply for an import certificate to import a medicinal product into the UK for veterinary use.
How to account for VAT on goods and services provided by registered health professionals, including doctors, dentists, nurses and pharmacists.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Submission dates and how the submissions using the EC decision reliance procedure work.
These published standards relate to a number of KPIs in the VMD Deliverables and KPI document.
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