On November 26, UtrechtInc is hosting a workshop on building a successful medical device development roadmap, organised by Stichting MedtechPartners.
If you’re developing a medical device and trying to understand MDR, this practical afternoon covers both the product and company sides of regulatory requirements, led by two experts.
Programme:
13:00 Introduction by Joep Welschen, Stichting MedtechPartners
13:15 Value development & regulatory requirements – product focus
14:45 Regulatory requirements & milestones – company focus
16:00 Closing
Speakers:
Jan-Bart Hak – Director Medical Devices Europe at ProPharma Group, with over 20 years of experience in clinical research and regulatory affairs for medical devices.
Willem Baelde – Founder of Baelde Consulting, specialising in quality and regulatory management for medical device companies in highly regulated industries.
Stay after 16.00 for the UtrechtInc open community drinks and meet other founders.
📅 November 26 | 13:00 – 16:00
📍 UtrechtInc, Utrecht
🔗 Register here