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Medicines & Healthcare products Regulatory Agency (MHRA)

The Medicines and Healthcare products Regulatory Agency (MHRA) has advised medtech firms to designate a ‘responsible person’ ahead of Brexit, updating guidance it provided in February. Read more

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The MHRA has reiterated guidance on how medical devices will be regulated in the event of a no deal Brexit. Read more

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The UK will need to establish its own systems in parallel with that of the European Union for life sciences in the event of a No Deal Brexit, according to a report from the House of Commons Exiting the EU Committee. Read more

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A historical lack of transparency in the UK’s medical devices industry has led to debilitating consequences for patients, the government admitted this week. Read more

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Med-Tech Innovation Expo, the UK and Ireland’s leading showcase for medical design and manufacturing technology, will once again deliver a world-class speaker programme for 2,500+ visitors at the Ricoh Arena in April. Read more

Expo News

The MHRA has now released guidance on human factors for medical devices. Miranda Newbery, managing director of Inspired Usability puts the document under the spotlight. Read more

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The government has rejected calls to ban vaginal mesh implants after MPs debated its use to treat women affected by pelvic organ prolapse and incontinence following childbirth. Read more

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The government has rejected calls to ban vaginal mesh implants after MPs debated its use to treat women affected by pelvic organ prolapse and incontinence following childbirth. Read more

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The UK Medicines & Healthcare products Regulatory Agency has issued new guidance for medical device makers when taking human factors into account. Read more

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