Thermo Scientific Watson LIMS is the leading data management solution for late stage drug development and is found in 19 of the top 20 pharmaceutical companies around the world, delivering the functionality, flexibility and scalability that meets their needs.
- Full security and complete compliance confidence for enterprise-wide knowledge and collaboration
- Provides a system with all the 21 CFR Part 11 components for compliance, including integrated audit trail, e-Signatures and granular security
- Study data workflow improved with automation
- Allows a full bi-directional interface capability to analytical instruments, tracks shipments and samples through user-designed barcode labels, supports a wide range of analyses, and organizes study results in a unique document management system
- Includes automated assay acceptance and rejection tool
- Permits improved collaboration and data transmission between sites, systems and customers currently using Watson LIMS
- Enables robust, dynamic reporting
- Supports built-in reporting and document management system, with full chain of custody reports for sample tracking
- Includes a comprehensive regression calculation tool, complete with linear and non-linear algorithms and many weighting factors
- Includes key functionality specific to the bioanalytical laboratory
- Flexible protocol-based study design, assay/method standardization and management
- Integrated sample tracking and a configurable reassay decision tree
- More than 70 built-in interfaces to LC/MS, HPLC, ELISA, RIA, ICP/MS, multiplex and other instruments
- Supports a wide range of pharmacokinetic/toxicokinetic calculations
- Dramatically improved performance when creating the Design Summary report with a dramatic increase in speed
- Ability to include incurred samples within the same run as regular bioanalytical samples; separate Mandatory Repeats run no longer necessary with Incurred Sample Reanalysis built in
- Built-in data interchange with the company’s TSQ Series mass spectrometers, allows for direct data acquisition, peak re-integration, storage, archiving and reporting of raw data, all under the control of Watson’s centralized Oracle* database repository
- New plate acceptance criteria such as ratio of the LQCs to the NQCs or ratio of the HQCs to the LQCs and comparison of the result to acceptance criteria with Immune Response Module
