For applications where product quality or patient safety is a concern
The viewLinc 3.5 from Canadian firm Veriteq, now part of the Controlled Environments division of Vaisala of Finland, is aimed at pharmaceutical processors seeking continuous monitoring systems specifically geared to larger enterprises.
This continuous monitoring system can be used in FDA regulated, GxP compliant environments, and all applications where product quality or patient safety is a concern. It provides continuous records, 24/7 alarming, and automated reporting and is easily deployed for monitoring temperature, relative humidity, CO2, differential pressure, level, door switches, and more.
The viewLinc 3.5 continuous monitoring system for larger pharmaceutical facilities
ViewLinc 3.5 enhancements include:
This latest version of viewLinc continues to ensure gap-free data recording with triple redundancy — point-of-measurement, host server, and automatic data transfers.
Highly secure and audit-trail capable, it meets compliance requirements for 21 CFR Part 11, CBER, The Joint Commission, AATB, AABB, and other life science and technology regulatory and accreditation bodies.
