by Eric Hanig | May 15, 2025 | Uncategorized
We’re excited to announce that our 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...
by Eric Hanig | May 15, 2025 | Uncategorized
May 14, 2025 — Today we announced the launch of support for FDA 21 CFR Part 11 within our application. This new capability allows life sciences organizations to seamlessly meet the stringent electronic records and electronic signatures requirements set forth by the...
