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Did you mean appropriate product
A form of IP that extends the protection of patented active ingredients present in pharmaceutical or plant protection products.
This toolkit is for Innovation Passport holders following the Innovative Licensing and Access Pathway (ILAP) and provides activities to support the design and development of medicines.
How a marketing authorisation holder should report a defect with a veterinary medicine.
Labelling rules for businesses in Great Britain (England, Scotland and Wales) and retailers in Northern Ireland, for certain agri-food products moved under the Northern Ireland Retail Movement Scheme.
Guidance for suppliers and dealers.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
How to import plants, fruit, vegetables, cut flowers, trees, seeds and used agricultural machinery to Great Britain (England, Scotland and Wales) from the EU, Liechtenstein and Switzerland.
How to comply with the requirements on promoting medicines to the public and to prescribers and suppliers of medicines.
Food and drink labelling and packaging regulations - what you must show, warnings, health and organic labels and packaging standards.
Find out if you need to use the UKCA (UK Conformity Assessed) marking on products you manufacture or handle.
Find out what a composite product is, and how to import or move composite products from the EU to Great Britain.
Using an ecological momentary assessment to evaluate your digital health product.
How to import animals and animal products to Great Britain (England, Scotland and Wales), the Channel Islands and the Isle of Man from non-EU countries.
Find out the rules to establish the country of origin of imported and exported goods and to help identify goods which qualify for lower or no Customs Duty.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Your purchasing strategy must show you’ve considered commercial and technology aspects, and contractual limitations.
When a material is waste, is a by-product or meets ‘end of waste’ status.
How to use a quasi-experimental study to evaluate your digital health product.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
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