meddevo
meddevo is a compliance platform built for medical device and IVD manufacturers. Its eTD solution automates regulatory workflows, CAPAs, and documentation to meet standards like EU-MDR, EU-IVDR, and ANVISA. It helps streamline compliance and future-proof your regulatory processes.
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meddevo Overview
meddevo is a specialized regulatory compliance platform designed for medical device and in vitro diagnostic (IVD) manufacturers. As a true vertical solution, its eTD (electronic Technical Documentation) platform streamlines the entire regulatory affairs process—automating workflows, tracking CAPAs, and enabling real-time monitoring. meddevo ensures that all technical documentation remains current and fully aligned with international regulations such as EU-MDR, EU-IVDR, and ANVISA. With built-in tools for change management and future-proof compliance, it empowers manufacturers to maintain global market readiness, reduce manual workload, and improve audit preparedness, all while enhancing transparency and efficiency in product lifecycle management.
Features
Automated Electronic Technical Documentation (eTD) Workflow
Regulatory AI Assistant
eSubmissions for Country Registrations
Integrated Post-Market Surveillance (ePMS) Management
meddevo Pricing Overview
meddevo Score
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FAQs
meddevo is a regulatory compliance platform designed for medical device and IVD manufacturers, focusing on automating and digitizing the entire regulatory affairs process.
Both startups and established corporations in the medtech industry can utilize meddevo to manage regulatory compliance efficiently.
As of now, meddevo does not offer a free trial. Interested users should contact the company directly for more information.
Yes, meddevo is designed to be customizable, allowing companies to tailor the platform to their specific regulatory requirements and workflows.
meddevo offers various support options, including email/help desk, FAQs/forum, knowledge base, phone support, 24/7 live representative, and chat support.
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