Data Integrity is not a new regulatory requirement, but important throughout your entire endotoxin testing process.

Do you know if you’re compliant in your endotoxin testing?

Our new White Paper guides you through a risk-based approach questionnaire using Failure Mode and Effect Analysis (FMEA) and helps you identify risks that may be inherent in your current workflow.

Topics include:

- How to document your data flow - How to build an audit trail and data review process