MedTech Summit 2023 – Speaking Engagement

Celegence invites you to join us for MedTech Summit 2023: The Flagship Regulatory Event for the Medical Device and In Vitro Diagnostic Industry taking place in Brussels, Belgium from 19 – 23 June 2023.

This event brings EU Commission, Competent Authority, Notified Body, and Medical Device and IVD industry experts together to discuss the evolving global regulatory landscape and share best practices.

What: Presentation on “Is the EU MDR Extension a Blessing or a Curse?”
When: Monday, 19 June 2023 15:05 – 15:35 CET/CEST (Cent Europe Summer, GMT+2)
Where: Hybrid Event
In-Person: Sheraton Brussels Airport Hotel, Brussels, Belgium
Digital Experience: As a hybrid event, delegates have the option to attend either in-person or digitally. All in-person presentations which take place in Brussels will be recorded and made available on-demand for 10 working days on the MedTech ConnectMe platform, and then for up to 12 months on the MedTech Streamly platform.
How: Register here
Why: Join this session to better understand the effects of the EU MDR extension to manufacturers, notified bodies, Brexit, how to deal with it and what medical device manufacturers must do to stay compliant.

This session will be led by Celegence’s RA/QA – Medical Devices SME, Joseph-Richardson Larbi.

MedTech Summit 2023 features 8 cutting edge topic streams covering EU MDR/IVDR, Clinical Investigations, Post-Market Surveillance, Software/AI, Biocompatibility, Law & Compliance, and Global Market Access.

Take a look at the full MedTech Summit 2023 agenda at a glance to see how you and your team can benefit!

Celegence is excited to be a conference sponsor at MedTech Summit 2023 and invites you to join us between 19 – 20 June 2023 at Booth 16.

• Joseph has 20 years of experience in medical device life cycle management and quality management systems (certified to ISO 13485, ISO 9001 & ISO/IEC17025).
• His key expertise includes the preparation and maintenance of technical files, product safety and vigilance reporting, clinical evaluations, risk assessment, regulatory audits, CE marking, and notified body opinion submissions.
• Medical device industry – Joseph has experience in diabetes management devices, nicotine replacement therapy (NRT) devices and pressurized metered dose inhalers (pMDI).
• Joseph has worked for small, medium, and large Biotech companies such as Roche, OBG Pharmaceuticals, and Kind consumer Ltd.

• What does the extension mean to Manufacturers?
• What are the pitfalls to avoid during the extension?
• Learn how notified bodies are dealing with the extensions – common challenges and advice.
• What is the impact of the extension for legacy versus new products?
• What does this mean for Brexit? How will Switzerland act?

Visit us at Booth 16 for complimentary consultations with Celegence’s experts throughout the event, including hands-on demonstrations of our exclusive technology for EU MDR & IVDR compliance – CAPTIS™

To learn more, reach out to info@celegence.com or contact us online or simply stop by the booth in the exhibitor area to meet with us. We hope to see you there!