Understanding MHRA regulation for software and devices – techUK member webinar

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