Laboratory Content ManagementMany companies struggle with the complexities of content management. Managing volumes of binders full of data, file cabinets and shelves of paper can be a daunting task, often resulting in significant delays in getting your laboratory equipment from the receiving dock to production. Manual development of instrument qualification protocols and routing for approval prior to execution and review post-approval can add weeks to the commissioning of your equipment into production.
Hybrid systems with combinations of paper records with “wet” signatures which must be manually scanned into content management systems often result in records stored in paper and electronic versions with different signatures which can create uncertainty about which documents constitute your official documents of record.
USDM & Agilent’s team of content management experts can assist you in improving lab efficiency, quality and control with a comprehensive, integrated electronic content management (ECM) system providing:
- Paperless management of validation and qualification documentation
- Network-based storage and retrieval
- Faster, more accurate data acquisition and analysis
- Increased collaboration and simplified data sharing
- Automated validation/qualification protocol development, execution and electronic review and approval
- Electronic tracking and management of out-of-tolerance, deviation and incident investigations
- Application-based data security with tamper proof electronic signatures
- Agilent Compliance Engine (ACE)
- Content Management Systems
- Laboratory Information Management Systems
- Scientific Data Management Systems
- Electronic Lab Notebooks
