Webinar Date & Time
12 November 2026 from 11:00 AM to 12:30 PM (CET)
Webinar Overview
Published in March 2026, ISO 14155:2026 supersedes the 2020 edition and remains the global reference standard for the design, conduct, recording, and reporting of clinical investigations involving medical devices in human subjects.
This updated version introduces 25 significant changes covering key aspects such as ethics, informed consent, study planning, risk management, methodology, and adverse event management.
Designed for medical device manufacturers, CROs, clinical operations professionals, and regulatory affairs teams, this webinar will provide a practical overview of the major updates introduced by ISO 14155:2026 and discuss their impact on the planning, conduct, and oversight of clinical investigations. Participants will gain actionable insights to ensure compliance and successfully adapt their clinical development strategies to the new requirements.
Presenters
Carla Lippens
Clinical Project Manager
Complife France
Carla Lippens holds a PhD in Immunology rom the Faculty of Medicine of Geneva and has over eight years of experience in medical device clinical and regulatory affairs. She is currently working at the European company GBA COMPLIFE Group, where she serves as a Medical Device Project Manager and Global Coordinator of Medical Device Clinical Investigations. She supports manufacturers in the development of pre- and post-market clinical strategies, the management of international clinical investigations, and regulatory compliance with the European Medical Device Regulation (MDR) and the ISO14155. Based in France, Carla is also an active member of the Medical Device Working Group within AFCROs and EUCROF.
Cécile Train
Medical Device & Drug Development Director
ClinSearch (France)
Cécile Train, M.Sc. in Bioengineering, is a Senior Director specialized in clinical development for both pharmaceuticals and medical devices, with 25 years of experience in clinical trial management and team leadership. She is a recognized expert in clinical operations and scientific strategy, with extensive experience leading international projects across multiple therapeutic areas and a broad range of medical device technologies. Based in France, Cécile is also an active member of the Medical Device Working Groups of AFCROs and EUCROF.
Khalil Ben Yahia
Clinical partnership specialist
Datacapt (France)
Khalil Ben Yahia is Clinical Partnership Specialist at DATACAPT, a company providing an eClinical platform dedicated to CROs and medical device manufacturers. He is a pharmacist by training and has over 15 years of experience in clinical studies, working closely with CROs, sponsors, and clinical research stakeholders. Based in France, Khalil is also an active member of the Medical Device Working Groups of AFCROs and EUCROF.
Attendance Fee
€ 90,- for non-EUCROF members
€ 60,- for EUCROF members
Deadline for registration
11 November 2026 at 6 p.m. CET
How to register?
1) Go on the REGISTRATION PAGE and click on the orange button “GET TICKETS”
2) Check your order and click on the green “CHECKOUT” button
3) Fill in all the necessary information and validate your order
Confirmation
You will receive 2 confirmation emails:
A) One from Eventbrite with your invoice
B) One from “Eucrof” with all the necessary information to connect the D-Day!
Questions?
Should you have any questions about registration, invoices or connection, do not hesitate and contact us by email at webinar@eucrof.eu
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