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SoftMolecular®

SCC's SoftMolecular information management system enables pathologists, geneticists, and forensic scientists to manage data and analysis stemming from current molecular testing methods in order to generate accurate interpretations and meaningful reports. This robust, user-friendly, and intuitive workflow solution for the diagnostic genetics laboratory enables users to streamline workflows, interface with automated instrumentation, manage patient and family cases, track sample storage, and control inventory. SCC's Genetics Information Systems Suite™ products allow communication with other laboratories, whether they are separate technology-based departments or multiple sites

SoftMolecular empowers users in all aspects of the genetic testing process - including direction of workflows through testing protocols, data transfer with automated equipment, management of samples, and tracking of inventory levels. SoftMolecular's intuitive workflow functionality enables users to track cases through DNA/RNA determination, amplification, detection, analysis, and interpretation. The robust reporting functionality found in the SoftMolecular module gives users an accurate, user-friendly data analysis and results reporting capability that facilitates comprehension of results from complex testing. Features, such as enterprise-wide reporting, enable users to track completion of tests including remaining/pending tasks, while daily manager worklist queues assist managers in keeping their technologists informed about daily fluctuations of workload

SoftMolecular offers seamless integration and interfacing with sequencing and fragment analysis instruments. These interfaces replace manual data transfer reducing resource investment and the inherent error rate associated with manual processes. This results in not only in greater efficiency and accuracy but also provides efficient data management and minimal loss due to human error.

Features
Benefits
  • Image attachments for each sample or per worksheet
  • Patient information and testing data can be easily accessed and referenced in a paperless environment. Therefore, patient files or logs are not required, which results in laboratory space and/or record storage expense savings
  • Ability to rerun an entire batch or auto-assign a specific sample to the next pending batch with a single click of the mouse
  • Enables users to quickly and easily manage repeat testing so these repeat tests avoid the delays or mismanagement that can occur with manual process management approaches. This ensures the most optimal turnaround time, thus enhancing client satisfaction.
  • Ability to link controls to a sample or batch
  • Control documentation will be accurate, can be accessible per patient or batch, and will remain electronically linked for historical reference or investigation. Users no longer need to sort through manual logs or files in order to identify or trend control data for quality control troubleshooting.
  • Auto-calculation of master mixes with auto-deduction of volume from inventory
  • Reduction of manual calculations and inventory control leading to error-free calculations and effective inventory management
  • Rules-driven alerts or notifications based on client, patient demographic, test, or result parameters
  • Reduce paper or phone communications and ensure timely and accurate delivery of special instructions or critical information.
  • Auto reflex and/or auto rerun testing across technologies based on client-defined rules
  • Eliminates manual error inherent in manual reflex/rerun ordering and reduces turnaround time of tests.