Quality Assurance Solutions

31. Highly Potent And Complex API Contract Manufacturing 4/23/2024

    Equipped with a diverse array of scales, our seasoned experts possess the finesse and acumen necessary to tackle even the most intricate and potent API projects.

32. Detect Label Data And Quality Defects On Round Product 8/29/2023

    V15 Label Inspection 360° System

    Compact, efficient, and reliable. This space-saving solution detects label data and quality defects on round products. Six image sensors are enclosed in a compact design that can easily be installed over existing conveyors. The V15 can be extended with top and bottom cameras.

    100% Automated Label Inspection 360°

    This cost-effective vision system is ideally suited to replace manual spot checks with 100% automated label inspection control for round products.

    Compliance Support

    The V15 supports consumer safety in offering documented label inspection in line with industry guidelines such as IFS and BRCGS.

    Reduce Waste and Prevent Recalls

    The V15 verifies labels to detect and reliably sort non-conforming products to avoid costly recalls due to false or missing declarations.

33. Scaling Methods Across Systems And Columns With A Column Calculator

    Scale your methods between different systems and across columns of different particle sizes and dimensions with the Columns Calculator. Walk through step-by-step instructions on how to use this tool.

34. Process Challenge Device (PCD®) Selection Guide 10/16/2025

    Explore how standardized PCDs improve sterilization reliability, reduce costs, and support regulatory compliance, as well as technology that offers more consistent EO sterilization validation.

35. The End-To-End Compliance Platform For Pharmaceutical Manufacturing 10/23/2024

    Optimize pharmaceutical manufacturing with real-time cleaning data, audit readiness, and automated compliance. This end-to-end compliance platform empowers companies to meet stringent regulatory standards.

36. Should You Digitalize Your CQV Process? 8/6/2024

    Legacy paper trails are a compliance nightmare.

    Missing documents, illegible handwriting, and inconsistent data leave you scrambling and vulnerable during audits. Digital CQV captures data and objective evidence in real time, ensuring a crystal-clear audit trail with time-stamped entries and electronic signatures that meet 21 CFR Part 11 requirements.

37. Manufacture High-Quality Products With Streamlined Compliance 6/26/2025

    Manufacture high-quality products with streamlined compliance.

38. Compliant Storage For Chemicals, Process Liquids, And Buffers 11/5/2025

    Maintain material quality and integrity with storage facilities compliant with ISO 9001, cGMP, and GDP standards. Features include real-time temperature control and HAZ-class segregation.

39. Enterprise Asset Management Platform 8/8/2025

    Discover an enterprise asset management system for life sciences that combines maintenance, calibration, and compliance tools to boost productivity, reliability, and GMP readiness.

40. Integration That Powers Real-Time Automation Across Your Enterprise 8/8/2025

    Unlock seamless integration that delivers real-time automation, compliance-ready data, and no-code configuration to streamline workflows, unify systems, and scale without disruption.