Funktionalität für die Life Sciences, insbesondere mit Dokumentation für Kalibrierung und Compliance
Vereinfacht die Verwaltung von Ausrüstung, Gebäuden sowie von mobilen und IT-Assets auf einer einzigen Plattform sowie die vollständige Einhaltung der Bestimmungen der FDA (Food and Drug Administration, USA).
Konsolidiert Lösungen unter einem Dach - Ressourcen- und Servicemanagement, Kalibrierung, mobile Kalibrierung, CAPA-Unterstützung - und kann mit RFID, SCADA-Systemen und LIMS integriert werden.
- FDA-konform gemäß 21CFR, Teil 11.
- Vollständige Funktionalität für Kalibrierung und mobile Kalibrierung.
- Unterstützung für CAPA (assetbezogen).
- Ermöglicht die Dokumentation der Compliance-Unterstützung (Compliance Assistance Documentation) in Validierungsprojekten.
- Berücksichtigt alle Arten von Assets, einschließlich aller Ressourcen mit IP-Adressen (z. B. SCADA, PLCs usw.).
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| Features | Advantages | Benefits |
|---|---|---|
| Industry specific capabilities | Provides industry specific capabilities to support life sciences and pharmaceutical manufacturing business requirements, such as regulatory compliance with FDA (21 CFR part 11 for support of electronic signatures and electronic audits), Calibration of instruments, tools & measurement equipment and standards, support for asset-related CAPA processes and support in Validation projects by providing Compliance Assistance documentation. | Aligns with the business needs and provides a greater fit out-of-the-box. |
| Rational consolidation | Allows organizations to consolidate multiple asset management solutions for production, facilities, transportation and IT assets into a single and common platform and database. | Lowers total cost of ownership for IT departments while providing a common platform for all EAM users. |
| Internet architecture | Provides a standards based, Java 2 Enterprise Edition (J2EE) certified platform that is Service Oriented Architecture (SOA) enabled. | Easy to use and easy to learn solutions that integrate easily with other SOA applications. |
| Risk Management | Supports compliance with government and industry regulatory requirements and helps achieve service level agreements (SLA). | Allows organizations to track regulatory compliance of all assets. |
Business benefits
IBM Maximo for Life Sciences helps manage equipment, facilities, mobile and IT assets on a single platform and be fully FDA compliant.
Product requirements
The product requirements and configuration matrix apply to the following products: IBM Maximo Asset Management, Tivoli Asset Management for IT, Tivoli Change and Configuration Management Database, Tivoli Provisioning Manager, IBM Tivoli Release Process Manager, Tivoli Business Continuity Process Manager, Tivoli Service Request Manager, Tivoli End Point Manager, and Tivoli Service Automation Manager.
IBM Maximo 7.1 Minimum Hardware and Software Requirements:
IBM® Maximo® uses an n-Tier architecture, which lets you deploy Maximo across one or more tiers. You can run Maximo on a single physical server or across multiple servers depending on the number of users and the hardware.
IBM Maximo and related products are part of a family of products with similar minimum hardware and software requirements. Use the link below to see the latest requirements for the Client Workstation, Application Server and Database Server.
IBM Maximo Software Configuration Matrix:
There are a number of combinations of operating systems, databases, applications servers, browsers, and report writers. Use the link below to access the current configuration matrix for the Maximo and the rest of the related family of products. This link includes configurations, languages, and platforms details
- Minimum Requirements And Software Configuration Matrix For IBM Maximo And Related Family Of Products
Additional Usage Restrictions:
Learn more about additional Usage Restrictions that may apply to this product. For more details, please refer to the Announcement Letter for the respective product.
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