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The rules that manufacturers and importers of fertilisers need to follow when trading in the UK.
The MHRA register of licensed manufacturing sites: manufacturer specials - human (MS) and manufacturer specials authorisation - veterinary (MANSA) only.
Factsheet from the Carbon Trust for manufacturers of energy-saving products who want their products to qualify for the Energy Technology List.
Guidance to help applicants and licence holders get and maintain a manufacturer licence - MHRA guidance note 5.
Estimates for UK manufacturers' sales by product (ProdCom) for 2020.
Producer responsibility laws in the UK cover packaging, electrical and electronic equipment (EEE), batteries and end of life vehicles (ELVs).
Estimates for UK manufacturers’ sales by product (ProdCom) for 2022, including 2021 final sales data.
Register a new manufacturer's mark and access lists of approved and inactive measuring container bottles (MCB) marks.
Guidance for UK wholesalers and manufacturers on how to import human medicines including unlicensed medicines, how to apply for a licence and how much it costs.
How to place CE marking on your product, how to identify UK requirements relating to construction products, and how to apply to be a UK Notified Body or Technical Assessment Body.
Supplier declarations are where your UK supplier provides you with information needed to prove the origin of your goods for preferential rates of duty between the UK and other countries.
Product security factsheet accompanying the Product Security and Telecommunications Infrastructure Bill, outlining the problems the Bill will address and how.
Advice for manufacturers of Class I medical devices for placing products on the UK market
To apply for a manufacturer licence, complete the appropriate form. Applications for a manufacturer licence will be payable on invoice.
Information about the EU Regulations and their implementation in Northern Ireland
How to get fast-track approval of medical devices during COVID-19.
Estimates for UK manufacturers' sales by product (PRODCOM) for 2019.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
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