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Marketing authorisations granted in 2024
Guidance for the pharmaceutical industry on how to apply for an authorisation to place a veterinary medicine on the UK market or part of, or to expire one.
This guidance is designed to help UKHSA customers and partners to navigate engaging and working with us and to signpost upcoming events and opportunities.
How we work with buyers and suppliers to improve the way technology is bought across government and the public sector.
How to market eggs, including rules on registration, egg marking, salmonella control and egg marketing inspections in England and Wales.
Find out about the Fruit and Vegetables Aid Scheme.
This webinar looks at the information an organisation makes available to clients, or potential clients, and how the consumer's expectations can be met.
How to comply with the requirements on promoting medicines to the public and to prescribers and suppliers of medicines.
The MHRA will review applications for orphan designation at the time of a marketing authorisation (MA) or variation application.
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
The government introduced a ‘Cloud First’ policy in 2013 for all technology decisions.
These published standards relate to a number of KPIs in the VMD Deliverables and KPI document.
Information about what to do if you receive a warning or advisory letter from the CMA.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Guidance on the European Union regulation on explosives precursors, including licensing, labelling and reporting suspicious activity
Business potential of producing crops for non-food markets, how and where to grow them and details of organisations providing grants.
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