Pharmaceutical Grade & Loaded with Advanced Data Integrity Features. Specifically designed for the pharmaceutical & life science industries. Automates the collection and export of compendial metadata to provide complete User and Data Integrity in compliance of 21 CFR Part 11. Includes a User Audit Trail, onboard sample memory buffer for 50,000 records, audit reports, and more! Meets all requirements and recommendations for ISO 14698-1 and BS EN 17141. Easily exports sample records to Lonza MODA, and other LIMS. More critically, users can expect to eliminate or mitigate deviation reports and investigations due to interval calibration out-of-tolerance conditions.