Product Information
What is Meddevo?
🚀 Manufactured for medical device and IVD manufacturers. 🤖 Simplify and automate your regulatory processes. 📜 From CAPA to dynamic workflow management. 🌍 Ready for EU-MDR, EU-IVDR, ANVISA, and BEERTEH.
📖 Founder's story: https://www.5-ht.com/en/media/blog/the-future-of-technical-documentation-automation-in-the-healthcare-sector
🇩🇪🎪 Official exhibitor of the German State at WebSummit 2023: https://websummit.german-pavilion.com/en/sites/exhibitors/100753
How to use Meddevo?
Meddevo is a solution for medical device and IVD manufacturers, automating technical documentation and digitizing regulatory processes to significantly reduce compliance burdens.
Core Functions of Meddevo
Automated technical documentation
Digitized regulatory affairs processes
CAPA and dynamic workflow management
Regulatory AI-assisted medical writing
UDI (Unique Device Identification) management
Electronic Clinical Evaluation Report (eCER)
Usage Scenarios of Meddevo
- Regulatory compliance for medical device and in-vitro diagnostic manufacturers
- Manage and automate technical documentation
- Reduce regulatory burden and improve efficiency
- Comply with international standards like EU Medical Device Regulation (EU-MDR)
- Leverage AI-assisted medical writing
Common Questions about Meddevo
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