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The Chancellor will meet top regulator bosses in Downing Street today (Monday 17 March) as she unveils an action plan to deliver on the pledge to cut the administrative cost of regulation on business by a quarter, make Britain the...
Use these general provisions to help you determine the origin of your products.
Use the case studies to help you decide when your goods may (or may not) go beyond insufficient production.
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Check what processes are considered as insufficient production under the Trade and Cooperation Agreement.
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
Researchers achieve 10x production cost savings for reduced activation steel
Guidance for manufacturers who source their own-branded products from another company.
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