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These temporary good manufacturing practice (GMP) flexibilities will be allowed to address the current exceptional circumstances
The official UK government website for data and insights on COVID-19.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Find UK trade data from HMRC. Look up data about imports, exports, commodities and traders.
Register your decision on the NHS Organ Donor Register. This will give your loved ones the certainty they need to support your choice.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
Information about how many laptops, and tablets and 4G routers we have delivered or dispatched to local authorities, and academy trusts and FE colleges.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
Find registered designs in the UK
Information on variants of the SARS-CoV-2 virus.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Check the tariff classification for double end studs with or without heads.
Information on OPSS product safety alerts, reports and recalls for unsafe products and resources for consumers, businesses and regulators.
A list of upcoming webinars on the UK’s approach to product marking and placing products on the market in Great Britain and Northern Ireland.
Product security factsheet accompanying the Product Security and Telecommunications Infrastructure Bill, outlining the problems the Bill will address and how.
The Export Control Joint Unit (ECJU) administers the UK’s system of export controls and licensing for military and dual-use items. ECJU is part of the Department for Business and Trade .
View designs registered in the designs journal from the last 25 years
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
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