Content Video
ValGenesis iOps™: SOP-Driven. Built for Accuracy. Fully Traceable.
0:11 Manual logbooks, inconsistent records, and disconnected workflows slow down teams and increase compliance risk.
0:18 It's time to boost the efficiency of your operations through capturing data in real time, whether online or offline.
0:27 iOps streamlines logs across cleaning, equipment, calibration, maintenance, and more—bringing clarity, accuracy, and control to every task.
0:37 Use customizable forms, enforce SOP-aligned workflows, and access your logs anytime, from any device.
0:44 iOps provides real-time traceability, built-in audit trails, and data integrity—keeping your operations inspection-ready.
0:53 ValGenesis iOps — for operational execution that’s connected, compliant, and always in control.
Summary
Manual logbooks and disconnected workflows create inconsistent records, slow execution, and raise compliance risk. ValGenesis iOps™ replaces paper-based logging with real-time digital capture, online or offline.
Standardize tasks with customizable forms and SOP-aligned workflows, then retrieve logs from any device. Built-in audit trails and traceability help keep operations inspection-ready.
Key Takeaways
• Capture operational data in real time, even when offline, to reduce delays and inconsistent records.
• Use configurable forms and SOP-aligned workflows to standardize execution across cleaning, equipment, calibration, and maintenance logs.
• Maintain inspection readiness with traceability, audit trails, and data integrity controls.
Who is this for
• Manufacturing operations managers and shift leads
• Quality assurance (QA) managers and compliance leads
• Maintenance and reliability managers (equipment upkeep)
• Calibration and metrology supervisors
• Cleaning and sanitation leads in regulated facilities
• Validation / CSV specialists supporting GxP systems
• Audit readiness and inspection preparation teams
Relevant entities and links
• 21 CFR Part 11 (Electronic Records; Electronic Signatures) — https://www.ecfr.gov/current/title-21/chapter-I/subchapter-A/part-11
• EU GMP Annex 11 (Computerised Systems) – European Commission PDF — https://health.ec.europa.eu/system/files/2016-11/annex11_01-2011_en_0.pdf
• PIC/S Guidance on Data Integrity (Data Management & Integrity in GMP/GDP) — https://picscheme.org/docview/4234
• MHRA ‘GxP’ Data Integrity Guidance and Definitions (March 2018) – PDF — https://assets.publishing.service.gov.uk/government/uploads/system/uploads/attachment_data/file/687246/MHRA_GxP_data_integrity_guide_March_edited_Final.pdf
