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Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Lists of standards that businesses can use to show their products, services or processes comply with essential requirements of legislation.
The CMA has accepted commitments offered by Google that address the CMA’s competition concerns resulting from investigating Google’s proposals to remove third-party cookies and other functionalities from its Chrome browser.
Using an ecological momentary assessment to evaluate your digital health product.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Get help classifying computers, inkjet and toner cartridges and their components.
Get help to classify electrical equipment such as communication equipment, cameras, and their parts and accessories.
Get help to classify textiles and which headings and codes to use.
Information on trade sanctions, arms embargoes and trade restrictions, including trade controls, transit controls and restrictions on terrorist organisations.
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