# MedDevo

> Regulatory documentation platform for medical devices and in vitro diagnostics (IVDs). MedDevo digitizes and automates technical documentation, compliance workflows, and regulatory processes for the EU MDR and IVDR.

## About

- [About MedDevo](https://meddevo.com/about): Company mission, vision, milestones, and impact stats
- [Team](https://meddevo.com/team): Leadership and team members
- [Contact](https://meddevo.com/contact): Get in touch
- [Jobs](https://meddevo.com/jobs): Open positions

## Products

- [eTD - Electronic Technical Documentation](https://meddevo.com/products/etd): Content-based technical documentation platform with 1,700+ structured data endpoints. Flagship product.
- [eTD Features](https://meddevo.com/products/etd/features): Detailed feature overview of the eTD platform
- [eIFU - Electronic Instructions for Use](https://meddevo.com/products/eifu): Digital platform for publishing and managing instructions for use
- [DocHub](https://meddevo.com/products/dochub): Secure document distribution portal for external stakeholders

## Solutions

- [Digital Standards](https://meddevo.com/solutions/digital-standards): Digitized regulatory standards management
- [Submission Management](https://meddevo.com/solutions/submission-management): Streamlined regulatory submission workflows
- [UDI Data Management](https://meddevo.com/solutions/udi-data-management): Unique Device Identification data management
- [Essential Notification Body Requirements (ENB)](https://meddevo.com/solutions/enb): Notified body requirements management
- [Clinical Evaluation](https://meddevo.com/solutions/clinical-evaluation): Clinical evaluation report automation
- [Risk Management](https://meddevo.com/solutions/risk-management): Automated risk management plans and reports

## Use Cases

- [Digital Technical Documentation](https://meddevo.com/use-cases/digital-td): Transitioning from static documents to structured data
- [Standard Management](https://meddevo.com/use-cases/standard-management): Managing regulatory standards compliance
- [Migration](https://meddevo.com/use-cases/migration): Migrating existing documentation to MedDevo

## Standards & Expertise

- [DIN SPEC 91509](https://meddevo.com/mdku/din-spec-91509): Standardized data model for digital medical device technical documentation
- [MDKU](https://meddevo.com/mdku): MedDevo Knowledge Unit — DIN SPEC 91509 validator and resources
- [Academy](https://meddevo.com/academy): Regulatory affairs training and education (coming 2026)

## Demo

- [Request a Demo](https://meddevo.com/demo): Schedule a live product demo
- [On-Demand Demo](https://meddevo.com/on-demand-demo): Watch a recorded product walkthrough

## Blog

- [Blog](https://meddevo.com/blog): Articles on regulatory affairs, medtech, and digital documentation

## Legal

- [Imprint](https://meddevo.com/imprint): Legal notice and company registration details
- [Privacy Policy](https://meddevo.com/privacy-policy): Data protection and privacy information
- [Terms of Use](https://meddevo.com/terms-of-use): Terms and conditions