ISO/DIS 18969 Clinical Evaluation of Medical Devices Training
Unlock the Future of Medical Device Compliance with ISO/DIS 18969
What the training will cover
- Learn from Florian Tolkmitt, one of the most known voices regarding Clinical Evaluation of Medical Devices.
Walk through the key principles, terminology, and processes defined in ISO/DIS 18969 for Clinical Evaluation of Medical Devices.
- Learn how to verify safety and clinical performance, and ensure sufficient clinical evidence across the device life cycle.
- Discuss how to align your Clinical Evaluation strategy – from pre-market data to Post-Market Clinical Follow-up – in line with upcoming regulatory expectations and global best-practice standards.
- Highly interactive session with room for questions.
Speaker
Regulatory & Clinical Evaluation Expert
PRO-LIANCE GLOBAL SOLUTIONS GmbH Managing Director
Florian Tolkmitt is Co-Founder & Managing Director of PRO-LIANCE GLOBAL SOLUTIONS GmbH. He is passionate about Clinical Evaluation of Medical Devices, driving innovation and excellence to ensure the highest standards and safer patient outcomes.
Additional information:
- Registration and webinar will be managed via Microsoft Teams. Billing and cancellation information will be sent to you via a separate email after registration.
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