Date: April 24th, between 10:00 - 16:00

Location: Bayes Meeting Room 3.57

Medical Device regulations can seem overwhelming, especially as they are constantly evolving to remain in line with wider legislation and end-patient needs. Failing to consider these regulations can lead to a premature end for any project, so it’s really important to get them figured out as soon as possible.

Luckily, we have help! Richard Hall will be offering 1 to 1 slots (lasting 45 minutes) to answer your questions concerning Medical Device Regulations.

Richard has worked in the medical device industry since 1993 and has held senior management positions within New Product Development, QC, QA and Regulatory Affairs. He is now Director of QMS Consultancy. In this role, he has helped over 60 companies to develop more than 100 medical products including medical devices from Class I – III & IVD’s from Class A – D and is named as inventor on two patents.

Richard has also written numerous product technical files and has been successful in gaining regulatory approval for multiple medical devices. As a trained lead auditor, he knows exactly what is necessary for a successful audit and has been the company contact for more than 85 notified body audits, the support he can offer throughout the audit process is invaluable.

He lectures at Imperial College London on Medical Device Regulations and holds an Expert In Residence position at the University of Oxford and Imperial.

Please do be aware that there are only limited slots available.

To secure your space, please click here to get in touch and let us know you're interested in a meeting.

You can also sign up below, and we will be in touch to arrange your timeslot.

As slots are limited- if you sign up but can no longer attend please do let us know as soon as you can- so that we can offer the space to someone else.