Data Integrity & System Security
Data integrity is about more than compliance with regulations; it is about protecting research and products for human use. In GxP applications, data often represents a significant investment in development, clinical trials, donated tissue, and the hopes of patients for a new therapy or drug. As in all other aspects of regulated industry applications, these processes require trustworthy systems to ensure patient safety.
- Webinar: Data integrity in pharmaceutical environmental monitoring - beyond bytes and signatures
- White Paper: Managing GxP environmental systems to ensure data integrity
“After installing viewLinc we were pleased... but it was during the hurricane that it really proved itself. Once we were able to return to work, we began analyzing conditions during the power outage. ...We verified and saved product that might otherwise have been needlessly destroyed because of the storm. As a result, our products reached patients without interruption, and the savings were huge.” Luis Johnson, Site Automation Engineer, Teva Pharmaceutical Industries
Data integrity in pharmaceutical environmental monitoring - beyond bytes and signatures
In this webinar you will learn how to maintain data integrity in software used in GxP-regulated operations. Along with best practices for managing environmental data, we provide an up-to-date overview of the current regulatory expectations for practices that ensure data integrity. Webinar includes a question and answer period where are regulatory expert answered questions on data management in GxP-compliant operations.
Key learning objectives:
- Review of recent guidance and documents
- Learn how to evaluate data integrity risks
- Discuss common pitfalls of data management in GxP applications
- Review best practices for ensuring and preserving data integrity
Managing GxP environmental systems to ensure data integrity
8 recommendations for establishing and maintaining good practices for data integrity. In this white paper, become aware of data management best practices for life science systems and explore an overview of regulatory expectations.
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