On demand webinar

What does the webinar cover?

The deadline for UKCA marking is fast approaching, and some changes happened in later 2022. This webinar gives an insight into the current state of play with information on new timeline extension and lessons learnt from an approved body perspective.
We discuss the importance of submitting applications to an approved body and give an overview of the process to UKCA Marking. We also touch on with the status of the new UK legislation and what this may entail.

Who should attend the webinar?

This webinar offers Approved Body insights for all people involved in working towards a UKCA application, whether you are a novice or have more significant experience of working with an approved body.

What will participants gain?

• Insight into the last updates on UK legislation for medical devices
• The future of the UK legislation
• Key Points to consider into applications for UKCA

Vishal joined BSI over 6 years ago and is currently the Head of the UK Approved Body and a Senior Regulatory Lead for Medical Devices. He is responsible for the regulatory oversight of the Medical Devices Approved Body and wider BSI strategy, policies, procedures, and documentation to meet the various legislative and designation requirements. Prior to his current role, he has been a Regulatory Lead, Technical Team Manager, Technical Specialist & Scheme Manager with expertise in Active Devices.

Vishal holds a Master in Medical Engineering from Queen Mary University of London and has over 10 years’ experience with medical devices working within industry, third party testing and Notified/Approved Bodies.