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Data, Freedom of Information releases and corporate reports
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Find out when you can zero rate books and other forms of printed matter.
Answers to frequently asked questions on Approved Document B including 2020 and 2022 amendments.
Get help to classify textiles and which headings and codes to use.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
The European Trade Mark and Design Network has produced a common practice for use when assessing the inherent distinctiveness of figurative trade marks containing descriptive and/or non-distinctive words.
Guidance for manufacturers, importers and distributors.
Information for wholesale dealer licence holders about the medicines put on the UK market for UK patients that they cannot export or hoard.
Get help to classify electrical equipment such as communication equipment, cameras, and their parts and accessories.
How to work out the VAT on building work and materials if you're a contractor, subcontractor or developer.
Find out how to work out VAT on supplies of staff including supplies made by staff bureaux.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Find out about other simplifications you can apply for with consignor or consignee status.
Functional Standards Common Glossary
Guidance for industry on flexible approaches we are taking on good distribution practices.
Get help to classify ceramic articles for import and export.
A guide to collecting data about your packaging. This is for UK organisations affected by extended producer responsibility (EPR) for packaging.
Hearing and inquiry notices and decisions for common land applications.
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