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Data, Freedom of Information releases and corporate reports
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Guidance for manufacturers, importers and distributors.
A form of IP that extends the protection of patented active ingredients present in pharmaceutical or plant protection products.
The duties and competence requirements for building regulations that clients, designers and contractors must meet.
If you're advertising or marketing, including direct marketing, you must be accurate and honest and follow the advertising codes of practice
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
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.
How to write requirements for services on the Digital Outcomes and Specialists framework
How you import from and export to Mexico.
This guidance provides information about permission in principle - a new planning consent route.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
An overview of the changes made to the Railways (Interoperability) Regulations 2011 that came into force on 1 January 2021.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
How you import from and export to Turkey.
How organisations can bid for contracts as a consortium, including the relevant requirements set out in the invitation to tender (ITT).
Guidance on the pre-application stage for Nationally Significant Infrastructure Projects.
Sets out the process for efficient and inclusive consultation of planning applications
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