Coding is an important consideration for CE certification of In Vitro Diagnostics (IVDs). Commission Implementing Regulation 2017/2185 established the codes for the designation of notified bodies in vitro diagnostic medical devices under Regulation (EU) 2017/746.
Join our webinar to learn about this coding system and how notified bodies use the codes to describe the individual qualification of the notified body personnel and the competences required for assessing a device. Our speakers will discuss how the correct coding is important for your application to SGS for CE certification.
Overall, this webinar aims to inform the attendee on the use and importance of coding under the IVDR, to help equip manufacturers with the necessary information to ensure the conformity assessment procedure is efficient and predictable and their products remain compliant to the higher standards set by the IVDR.
Agenda
Target Audience: The webinar is intended for in vitro diagnostic medical devices manufacturers – globally, including corporations and SMEs, start-ups, Person Responsible for Regulatory Compliance (PRRC), EU Authorized Representatives, Regulatory affairs managers and their team, Quality managers and their team, Technical directors and their team, R&D Managers and their team, and Validation Managers and their team.
Language: English
Cost: No Charge
Can't make a live session? Register now and receive a complimentary recording after the live event. For further information, please contact: KNGlobalMarketing@sgs.com