OBODUX | Medical Device Technical File Software

OBODUX helps medical device manufacturers efficiently create and maintain complete Technical Files for MDD, MDR, and FDA submissions.

Our platform automates key documentation workflows — including risk analysis (ISO 14971 / ISO 24971), clinical evaluation, verification and validation, labeling, and post-market surveillance.

With built-in regulatory guidance and AI-assisted tools, OBODUX ensures your documentation is accurate, consistent, and submission-ready — reducing time and cost in achieving global regulatory compliance.

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Links to add:

🌐 Website: https://www.obodux.com

💼 LinkedIn: https://www.linkedin.com/company/obodux/?viewAsMember=true

📩 Demo / Contact: hello@obodux.com