21 CFR Part 11 Compliance Statement for Logilab SDMS
This document presents the requirements set forth in 21 CFR Part 11, along with Agaram’s own interpretation of the requirements with respect to its product Logilab SDMS
Automation – The Way Forward to achieve Data Integrity. “Data Integrity is considered as the first and foremost requirement in a pharmaceutical quality system to ensure that the medicines are of the required quality”