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Departments, agencies and public bodies
News stories, speeches, letters and notices
Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
Senior Efficacy Assessor vacancies, working in the regulation of veterinary medicines.
Submission dates and how the submissions using the EC decision reliance procedure work.
Twenty packets of worming tablets seized at Border Force in Belfast.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Blogs where government organisations talk about their work and share information and ideas.
Register as a manufacturer, importer or distributor of active substances.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
How to apply for marketing authorisation via this new procedure.
The Foreign, Commonwealth & Development Office (FCDO) provides lists of English-speaking lawyers abroad to help British nationals find the legal support they need.
The Export Control Joint Unit (ECJU) administers the UK’s system of export controls and licensing for military and dual-use items. ECJU is part of the Department for Business and Trade .
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
From 1 January 2014 herbal smoking products will have Tobacco Products Duty charged on them unless they are to be used exclusively for medical purposes.
Guidance for local authorities, port health authorities and food traders on how to submit a sample for referee analysis.
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
The actions to take for sourcing medicines in different circumstances.
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