Key Elements of Quality Assurance
in the Good Laboratory Practice
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.
We invite you to download the detailed and informative white paper that will give you insights into the processes, integration points and best practices for implementing an integrated GLP and QA infrastructure.
Xybion provides software and solutions to companies operating in heavily regulated environments
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About Xybion Corporation
At it's core, Xybion provides a suite of compliance software, laboratory operations solutions, preclinical software and quality management software that are designed to support global companies operating in highly regulated industries. Today’s global companies need solutions designed to accelerate their unique business processes. Xybion specializes in the development and delivery of flexible enterprise solutions that can be easily configured, integrated, or deployed out of the box to deliver the capabilities you need.
Our total solution and deliver model includes a cross-functional, yet integrated platform designed to provide compliance, quality and risk mitigation in a pervasive manner while reducing the need to run and support disparate systems. On average, Xybion saves its customers 20-30% on IT hardware, software and maintenance costs related to GRC technology