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The guide, toolkit and further information for GB authorities with responsibility for consumer product safety.
This guidance provides an overview of the different tariffs for products exported to the UK under the DCTS, including how to identify commodity codes.
Use a separate statement of objection form for each Georgian GI product name you object to.
Information for manufacturers.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Guidance for healthcare professionals on managing specific medicines and medical devices and using them safely.
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.
How product specific rules are used to identify the country of origin when importing or exporting between the UK and EU.
How to display the legal name for your food product.
Use these general provisions to help you determine the origin of your products.
Find product safety alerts, unsafe products and recalls
Uses of fluorinated gases (F gases) that are banned or will be banned in the future.
A collection of guides for anyone working with animal by-products (ABPs), including how to process, transport, store and dispose of them.
How a marketing authorisation holder should report a defect with a veterinary medicine.
We advance prosperity by ensuring no viable UK export fails for lack of finance or insurance, doing that sustainably and at no net cost to the taxpayer.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
How to use a cost benefit analysis to evaluate your digital health product.
Find out which standards and regulations apply to your product and how to make sure you follow the right procedures.
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
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