RAPS Euro Regulatory Convergence Conference 2022 – Speaking Engagement

Celegence invites you to join us online for the RAPS Euro Regulatory Convergence Conference on 10-12 May. Come together with other European regulatory affairs professionals to discuss pressing regulatory topics and share best practices within the MedTech industry.

What: Training Session on “Major Pain Points and Solutions for Medical Device Manufacturers for EU MDR 2017/74 Compliance”
When: Thursday, May 12th at 13:00 PM – 13:30 PM CEST
Where: Park Inn by Radisson Amsterdam City West, La Guardiaweg 59, Amsterdam, 1043 DE
How: Register Here
Why: Join this session to better understand the major pain points of CER, QMS, UDI, registrations, technical file remediations and Post Market Surveillance for small, mid and large sized medical device manufacturers. Our expert will also describe how to address these pain points for EU MDR 2017/74 Compliance.

Designed exclusively for regulatory professionals by regulatory professionals, RAPS EU Convergence is the largest annual regulatory-focused event in the EU – celebrating and supporting the global regulatory community! The event unites key stakeholders and decision makers across all intersections of the regulatory field for three powerful days of professional development, interactive discussions and relationship building.

Celegence is excited to be an Innovator Sponsor at RAPS EU Regulatory Convergence this year! Celegence invites you to join us for the RAPS Euro Regulatory Convergence Conference on May 12th, 2022. Come together with other European regulatory affairs professionals to discuss pressing regulatory topics and share best practices within the MedTech industry.

This session will be led by Celegence’s RA/QA Subject Matter Expert, Joseph-Richardson Larbi.

• 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.

• Better understand the broad requirements and challenges posted by EU MDR
• Point to specific solutions in addressing the major challenges across different areas: CERs, UDI, Technical File Remediations etc.

Visit us at Booth 9 for complimentary consultations with Celegence’s experts throughout the event.

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