The Role of Empower 3 Chromatography Data Software in Assisting with Electronic Records Regulation Compliance

Regulated pharmaceutical and biotech laboratories are currently striving to meet compliance with 21 CFR Part 11, the U.S. Food and Drug Administration’s (FDA) rule governing electronic records and electronic signatures. The objective of this white paper is to discuss the 21 CFR Part 11 compliance readiness of Waters^® Empower^® 3 Software for the regulated scientific laboratory.