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How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to apply for marketing authorisation via this new procedure.
How traditional herbal medicines and homeopathic medicines will be treated by the MHRA.
Sources of advice and financial support for UK farmers exporting agricultural products to the EU and beyond
Guidance for the pharmaceutical industry on who can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
How to renew marketing authorisations for products granted through different routes and at different times.
Guidance for holders of Marketing Authorisations approved in Northern Ireland or the EU/EEA member states who want to bring a product to market in Great Britain.
How an innovative funding mechanism is saving lives by speeding up the availability of vaccines and making them affordable.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
The way you apply to licence biological products has changed
Guidance on applying to renew a marketing authorisation (MA) for a veterinary medicine.
Use the rolling review route when you want to submit your eCTD dossier in separate parts for pre-assessment instead of making a full consolidated document submission.
How to use a crossover randomised controlled trial to evaluate your digital health product.
Marking, labelling and marketing standards you must follow to import and export plant seeds, food and manufactured goods.
How to market forest reproductive material (FRM) for forestry purposes, including regulations, registration, master certificates and licences.
Guidance on the Genetic Modification Inspectorate (GMI) seed audit programme for companies in England that import, produce or market seed.
Leading food delivery companies will introduce enhanced security checks on their apps to prevent the market being abused by illegal workers, following discussions with the government.
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
How veterinary medicines can be advertised.
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