This member webinar will explore how the Medicines and Healthcare products Regulatory Agency regulates software and medical devices, clarifying when and how regulatory requirements apply across the product lifecycle. The session will outline pre- and post-market expectations and provide an opportunity for members to raise questions that will inform the development of joint industry guidance.

Key takeaways

  • Understand how regulatory requirements apply to software and medical devices
  • Clarify pre-market and post-market expectations
  • Explore regulatory considerations across the product lifecycle
  • Contribute questions to inform joint industry guidance

This webinar is relevant for members involved in regulated health technologies, including:

  • Organisations developing software as a medical device
  • Companies manufacturing or supplying medical devices
  • Regulatory, compliance, and product teams

Robert Walker

Robert Walker

Head of Health & Social Care, techUK

Rachel Kennedy

Rachel Kennedy

Programme Manager Health and Social Care, techUK

Lewis Stewart

Lewis Stewart

Programme Manager ‑ Health and Social Care, techUK

Viola Pastorino

Viola Pastorino

Junior Programme Manager, Health and Care Team, techUK

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techUK is helping its members navigate the complex space of digital health in the UK to ensure our NHS and social care sector is prepared for the challenges of the future. We help validate new ideas and build impactful strategies, ultimately ensuring that members are market-ready. Visit the programme page here.

 

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