This training is ideal for:
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R&D engineers and managers
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Quality & Regulatory professionals
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Biomedical or clinical researchers
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Product developers in healthcare
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Leadership in MedTech companies
Training information
- 1 day
- 23 October
Investment
The investment for the training is €995 per participant, excluding VAT.
Included are the training day, lunch and refreshments.
Other training possibilities
Not able to join the 23rd of October in Enschede? Here other opportunities to join:
- 20 November 2025, Eindhoven
- 22 January 2026, Enschede
Curious?
Talk to our academy advisorAI for MedTech
From theory to impact: AI as a smart co-pilot in medical device development
The MedTech sector is transforming. With growing complexity, regulatory demands, and pressure to innovate, artificial intelligence presents a unique opportunity—if used wisely.
This one-day, hands-on training is tailored for MedTech professionals looking to integrate AI safely and effectively into their development processes. You'll work with tools like ChatGPT, ChatPDF, Enago Read, Scholarcy, and Formly.AI—directly applied to daily tasks such as literature reviews, QMS documentation, and V&V workflows.
A basic working knowledge of MedTech is required. No prior AI or technical experience needed.
You'll learn to:
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Use AI immediately to boost your MedTech workflow
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Reduce time spent on repetitive work - without compromising quality
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Ensure compliance and data security when using AI
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Gain practical skills and confidence to apply AI effectively
Teaching professionals.
Bente Bouwmeester
Project Manager Medical Device Development
Bente is an enthusiastic professional with a background in Biomedical Engineering, focusing on medical product development. She is an analytic and pragmatic professional with a practical approach. She has experience with project management in a clinical setting, knowledge of the ISO 13485, ISO 14971 and 21CFR820 in a contract manufacturing environment.
Lisanne Karbaat
Regulatory Affairs Expert IVDR
Lisanne is an enthusiastic and thorough manager with extensive knowledge about regulatory requirements. She holds a masters degree in Biomedical Engineering and has several years of academic research experience using various in vitro diagnostic technologies. Her goal in medical projects is to let the build-up of documentation support the development of a device, so that people can bring safe and good products faster to the market.
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