Managing quality and compliance in a GLP (Good Laboratory Practice) environment is both a technical and process challenge. Quality management and GLP are not discrete solutions or processes and should work hand in hand in your environment. In this white paper, Xybion provides a foundation for understanding the concepts behind implementing and managing QA/GLP in a truly integrated fashion.
The US Food and Drug Administration relies on documented adherence to good laboratory practice (GLP) requirements by nonclinical laboratories in judging the acceptability of safety data submitted to the agency. Quality management processes can ensure you’re meeting these critical guidelines.