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The process for the simultaneous review of veterinary drug submissions by Health Canada’s Veterinary Drugs Directorate and the UK's Veterinary Medicines Directorate.
Find out about the process and costs to apply for Defra disinfectant approval.
Resources for local regulators.
The process for the simultaneous review of veterinary medicine submissions by Switzerland’s Swissmedic and the UK's Veterinary Medicines Directorate.
How to conform with the legal requirements for placing medical devices on the market.
How to apply for an authorisation to manufacture authorised veterinary medicines or medicines marketed under the Exemptions for small pet animals.
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
A range of tests are available from the majority of PHE regional clinical microbiology laboratories.
For manufacturers of long-term samplers and test laboratories who carry out testing of equipment.
How to set up a compost or biogas site, UK and EU standards explained, and alternative treatment methods for animal by-products (ABPs).
How to get fast-track approval of medical devices during COVID-19.
When tests to detect COVID-19 are commonly used (use cases) and what to consider when deciding which type of test to employ.
Resources to help anyone developing or running a digital health product to conduct an evaluation.
To assist sponsors and those conducting trials on implementing adequate oversight and monitoring processes for trials of investigational medical products.
Check for listed disinfectants for aquaculture; or apply to have your product listed.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
The laboratory provides diagnostic microbiological testing services for the examination of food, water and environmental samples.
Advice and information for MOT garages and testers.
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