Honeywell delivers electronic batch recording with tamper-proof audit trails that capture every process parameter, operator action and system event. Electronic signature functionality with role-based access controls prevents unauthorized changes and maintain compliance with FDA 21CFR Part 111. Version control systems track all application software changes, providing documented change management.
Additionally, TrackWise quality management software centralizes CAPA processes, audit management, deviation handling and document control, creating a unified system that simplifies inspections and accelerates corrective actions. These integrated digital solutions can help eliminate paper-based errors, reduce manual transcription mistakes and provide the documentation needed to demonstrate compliance.
1 - https://process.honeywell.com/content/dam/process/en/documents/downloads/Expeion-HS-03.pdf