meddevo eTD already comes with a lot of preconfigured regulatory knowledge. In form of folder structures, document templates and a smart content management.
Folder Structure Automation
Content Management
Document Automation
Preconfigured Regulatory Frameworks
EU-MDR 2017/745
Fully supported
Fully supported
Fully supported
EU-IVDR 2017/746
ANVISA - Brazil
PPE - Personal Protection Equipment
US-FDA
Extendable
Extendable
NMPA - China
TGA - Australia
IMDRF
+ Custom Frameworks
Extendable
meddevo is fully customizable to fit your regulatory and company needs. New country requirements are implemented fast by yourself or together with our regulatory experts.
Discovery Call & Get access
Take a look at the most sophisticated solution developed specifically for medical devices and IVD.
1. Discovery Call | 2. DEMO | 3. Workspace Setup
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The fastest and easiest way to digitalize your RA & QA