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The product and service community is for anyone who wants to discuss and learn about managing products and services in government.
How product specific rules are used to identify the country of origin when importing or exporting between the UK and EU.
Legal terms for veterinary medicines, marketing of non-medicinal products including medicinal words and phrases, how to complain.
This guidance provides an overview of the different tariffs for products exported to the UK under the DCTS, including how to identify commodity codes.
The guide, toolkit and further information for GB authorities with responsibility for consumer product safety.
Information for manufacturers.
Guidance for healthcare professionals on managing specific medicines and medical devices and using them safely.
Use these general provisions to help you determine the origin of your products.
How a marketing authorisation holder should report a defect with a veterinary medicine.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
Find out which standards and regulations apply to your product and how to make sure you follow the right procedures.
What animal by-products (ABPs) are, how to set up a site that uses them safely, the paperwork you need, and how to dispose of them.
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
Check the tariff classification for flavour pods.
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
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