Accruent Announces New IIoT-CMMS Integrations
Accruent has integrated its Maintenance Connection Computerized Maintenance Management System with the Meridian engineering document management system (EDMS) and vx Observe IoT platforms to facilitate interaction between maintenance, operations and engineering teams in the manufacturing sector.
Historically, CMMS users have grappled with the challenges of toggling between their CMMS platform and engineering document management or IoT software.
This has resulted in inefficiencies, particularly in accessing pertinent documents on-site, contributing to a fragmented user experience.
The integration of Accruent’s EDMS and IoT solutions with the Maintenance Connection CMMS creates a centralized platform for maintenance teams.
This empowers them to seamlessly access, visualize, update, and review all asset documentation in one place, crucial for reducing downtime, enhancing technician efficiency, and improving safety.
Additionally, the IoT integration provides teams effortless access to energy and remote monitoring, enabling early detection and resolution of potential asset failures.
By seamlessly integrating Maintenance Connection, Meridian, and vx Observe, we are empowering our customers with a comprehensive solution that not only boosts their operational efficiency but also helps them navigate the dynamic complexities of regulatory standards.
...[W]e are empowering our customers with a comprehensive solution that not only boosts their operational efficiency but also helps them navigate the dynamic complexities of regulatory standards.
"By seamlessly integrating Maintenance Connection, Meridian, and vx Observe, we are empowering our customers with a comprehensive solution that not only boosts their operational efficiency but also helps them navigate the dynamic complexities of regulatory standards."
The company further describes the integrations as the first in a range of broader initiatives to provide a comprehensive solution for organizations to achieve compliance under the 21 CFR part 11 Federal regulations on electronic records and electronic signatures (ERES) which have been introduced by the U.S.
Food and Drug Administration (FDA).