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Immigration staff guidance on the powers and obligations related to the seizure and interrogation of digital media under the Data Protection Act 2018 (DPA).
We are consulting on a draft code of practice containing guidance about the powers in sections 37(1) and 41(1) of the Police, Crime, Sentencing and Courts Act 2022.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Information and guidance on a range of medical devices for users and patients.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
Get help to classify cigarettes, cigars, raw tobacco, smoking tobacco, tobacco for heating and nicotine substitutes for import and export.
Order a certificate of free sale to export medical devices outside the UK.
How to get fast-track approval of medical devices during COVID-19.
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