How CMMS Helps Medical Device Manufacturers with Regulatory Compliance
Like all life science organizations, medical device manufacturing companies are held to strict standards set by the United States Food and Drug Administration (FDA) [...]
21 CFR Part 11 Compliance: A Quick Guide
Pharmaceutical companies, medical device manufacturers, labs, and other life sciences organizations need to be 21 CFR Part 11 compliant. The right maintenance software can [...]
Why GMP and GLP Compliance Matter in Manufacturing
In drug discovery, chemicals must undergo thorough testing before they can be safely administered to the public. It's critical to prevent the cross-contamination of drug [...]