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Ryden Launches Support for FDA Premarket and Postmarket Cybersecurity Guidance

by Eric Hanig | Jun 26, 2025 | Uncategorized

Bringing AI-Powered Gap Analysis to Medical Device Security Compliance At Ryden Solutions, we’re proud to announce that our platform now provides comprehensive support for the FDA’s Premarket and Postmarket Cybersecurity Guidance—a critical step forward for...

Ryden Adds Health Canada SOR/98-282 and ML-Enabled Medical Device Guidance Support

by Eric Hanig | May 29, 2025 | Uncategorized

Chicago – May 29, 2025 — Ryden, the AI-powered compliance intelligence platform, today announced the addition of Health Canada SOR/98-282 and the agency’s latest Machine Learning-Enabled Medical Device (MLMD) guidance to its regulatory automation engine. This...

Ryden Releases Support for FDA 21 CFR Part 11 Compliance in its AI Compliance Platform

by Eric Hanig | May 14, 2025 | Uncategorized

May 14, 2025 — Chicago, IL — Ryden, a leading provider of AI compliance technology, today announced the launch of support for FDA 21 CFR Part 11 within the Ryden application. This new capability allows life sciences organizations to seamlessly meet the stringent...

Ryden Adds EU MDR Compliance Support to Streamline Submissions and Audits

by Eric Hanig | May 1, 2025 | Uncategorized

We’re excited to announce that Ryden AI’s continuous gap analysis platform now supports the European Union Medical Device Regulation (EU MDR) QMS requirements — a major milestone that enhances our platform’s ability to help medical device manufacturers navigate...

Ryden Announces Support for ISO 13485:2016, Strengthening Commitment to Medical Device and Life Science Quality

by Eric Hanig | Apr 21, 2025 | Uncategorized

April 21, 2025 – Ryden is proud to announce its support for ISO 13485:2016, the global standard for medical device quality management. This milestone reinforces Ryden’s commitment to helping manufacturers meet stringent regulatory and quality requirements....

Ryden Introduces Comprehensive Compliance Bundle for Life Sciences

by Eric Hanig | Apr 21, 2025 | Uncategorized

April 21, 2025 – Ryden is streamlining regulatory compliance for life sciences with the launch of a comprehensive compliance bundle that integrates five key regulatory frameworks. This bundled approach simplifies compliance management for medical device and Life...

Ryden Launches Worlds first AI for Life Science Audits and Compliance

by Eric Hanig | Apr 21, 2025 | Uncategorized

April 21, 2025 – Ryden is revolutionizing the life sciences industry with the launch of the world’s first AI-driven solution for audits and compliance. This groundbreaking technology is designed to help pharmaceutical, biotech, and medical device companies streamline...
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