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Detailed guidance, regulations and rules
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Consultations and strategy
Data, Freedom of Information releases and corporate reports
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
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.
NHS Business Services Authority contact number for ordering prepaid prescriptions for 3 or 12 months at a cheaper rate than single prescriptions
Information on carrying medicine containing controlled drugs for individual travellers entering or leaving the UK.
Information about how to register your homeopathic medicinal product through the Simplified Homeopathic Registration Scheme or the UK Homeopathic National Rules Scheme
Controlled drugs and precursor chemicals licensing fees information for individuals and companies.
Submission dates and how the submissions using the EC decision reliance procedure work.
Information and guidance on a range of medical devices for users and patients.
Things to consider when buying and using products.
How test manufacturers or distributors can apply for approval of their tests to sell on the UK market.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
VAT and other taxes on shopping and services, including tax-free shopping, energy-saving equipment and mobility aids.
Procurement options available from the Crown Commercial Service for the public sector.
Pharmacovigilance system requirements
Apply for and maintain registrations for the brokering of human medicines.
Information about the EU Regulations and their implementation in Northern Ireland
The actions to take for sourcing medicines in different circumstances.
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