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How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
How the MHRA makes decisions on whether a borderline product is a medical device and which risk class should apply.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
Temporary export bars have been placed on two paintings by 18th century Italian artist Agostino Brunias
How to conform with the legal requirements for placing medical devices on the market.
To properly classify and manage waste, you must identify when EEE becomes WEEE.
Information about medical devices that the public can buy for personal use and how we make sure they are safe and effective.
Guidance on defining intended purpose for Software as a Medical Device (SaMD), to help SaMD manufacturers in meeting their statutory obligations.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
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