Say goodbye to boring
manual work
- Highlights
- — RegulatoryAI
- — eTD Content Management
- — MDR / IVDR Ready
- — Automation & Monitoring
- — Document Management
- — Approval Workflows
- — Multilanguage
- — meddevo University
- Additional Highlights
- — RegulatoryAI
- — eSubmissions
- — Custom Processes
- — REST API Options
- — eIFU Automation
- — Dedicated Success Manager
- Highlights from PRO +
- — Custom SLA
- — Multiple Workspaces
- — API Management
Content, Documents, Folders
ISO 27001/27017/27018/9001
Some of the most frequently asked questions
Yes. We will walk you around and then give you the keys to click around!
Yes. It is reserved for start-ups that do not yet have a certificate. All information on the start-up program is available from the team.
Yes. At any time. We only use open data formats. It's your data and documents. You have complete control over them.
Yes. The meddevo Platform offers a REST API to connect to other systems.
Servers are fully certified according to ISO 27001/27017/27018/9001. Regular Penetration & Security Tests are performed.
The entire platform is pre-validated according to ISO/TR 80002-2. However, the system can be customized according to your needs and delta validation can be performed.
Yes. Even though meddevo is already preconfigured and can be used immediately, the system has been developed in such a way that you can customize it to the needs of the company very easy. We are happy to help.
Our customers have products in all risk classes. I, Im, Is, Ir, IIa, IIb, III. Be it implants, active medical devices, or simpler products.
Your data is located in Frankfurt, Germany. However, other location around the globe are possible.
The team consists of people who not only know meddevo very well, but also have years of experience in medical devices. You can access the support team directly in the software.
