Medical Devices Regulatory Specialist
Medicines and Healthcare products Regulatory Agency (MHRA)
Elaine Grimes is the policy lead for international reliance within the innovative devices team at the MHRA. This would enable certain devices to undergo a streamlined review process compared to the UKCA conformity assessment, due to reliance on assessments that have already been performed by comparable regulators. She has also spent 10 years working in research of orthopaedic devices and biowearable sensors, focusing on regulatory requirements and biocompatibility, and has a PhD in bioengineering.
Scaling the Pond: Routes to Market in the UK and Switzerland
Thursday, October 9, 2025
4:30 PM - 5:30 PM EST