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Guidance on defining intended purpose for Software as a Medical Device (SaMD), to help SaMD manufacturers in meeting their statutory obligations.
How the MHRA makes decisions on whether a borderline product is a medical device and which risk class should apply.
When military end-use export controls apply and to which destinations.
The UK's regulatory framework for strategic export controls and the circumstances where you might need an export licence.
To properly classify and manage waste, you must identify when EEE becomes WEEE.
The guide, toolkit and further information for GB authorities with responsibility for consumer product safety.
When a material is waste, is a by-product or meets ‘end of waste’ status.
This guidance is intended to support individuals interested in conducting a field trial, including the application submission process.
Controls on the brokering of goods that could be used as parts or accessories for weapons of mass destruction and need an export licence.
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