Conformity of standards and requirements

Through a variety of measures the user has the possibility to monitor precision and accuracy of measurements fully automatically. He is enabled to generate a GLP confoming documentation of all analytical data. This way a comprehensive quality assurance is guaranteed.

Conformity to FDA 21 CFR Part 11 is often a must for modern analysis software. The functions integrated in WinASPECT^® PLUS ensure data security as well as the reliability, lucidity and traceability of all actions throughout the measuring time. Comprehensive user management, an electronic signature facility and the Audit Trail satisfy the requirements of FDA 21 CFR Part 11.