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....
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...
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...
