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CaliberLIMS

Score7.7 out of 10

6 Reviews and Ratings

What is CaliberLIMS?

CaliberLIMS is an LIMS system designed to meet regulatory compliance requirements. Equipped with multiple modules to choose from, including a built-in ELN and integrated software like Batch Record Management (CaliberBRM), Electronic Logbook ( CalibereLog), Document Management System (Caliber DMS), and Quality Assurance Management System (CaliberQAMS), Caliber LIMS aims to serve as the best laboratory partner on the path to digital transformation.

Categories & Use Cases

Media

CaliberLIMS

CaliberLIMS review

Use Cases and Deployment Scope

CaliberLIMS is the best laboratory tool used in the quality control laboratory for testing and recording of the analytical data for chemical testing and microbiological testing with 21 CFR part 11 compliance. CaliberLIMS enables the laboratory with a paperless system and maintains the integrity for regulatory compliance. Interface with equipment, fetch the raw data to the system, and auto-update the results to avoid transcription errors.

Pros

  • Equipment interface
  • Microbial Testing
  • Stability management
  • Media Management
  • Culture Management
  • Chemical Management
  • Specification Management
  • Column Management
  • Environmental Monitoring
  • Electronic log books
  • Certificate of Analysis for batch release

Cons

  • Test incharge profile simplification
  • Environmental monitoring module
  • Faster Equipment interface

Return on Investment

  • Reduce the resource for paper printing, archival and retrieval.
  • Less paper storage requirement due to paperless system.
  • Faster Data analysis and reduction in the review time.
  • Online data review and avoid chances of paper missing.
  • Anyone can review or access the data from anywhere.

Usability

Alternatives Considered

Nova-LIMS

CaliberLIMS one stop solution for QC sample management

Use Cases and Deployment Scope

CaliberLIMS is used to track all QC sample issuance and result so it can help to view as well as review reported result of QC sample in LIMS during proceeding next step of manufacturing and/or for batch release. It also help to track/view QC result data of batches for various purposes like preparation of cleaning validation report, process validation report and to review QC result for batch release.

Pros

  • QC result recording
  • View and managing reported result
  • Review of QC data and authorization of the same in LIMS
  • Managing QC result online in one place

Cons

  • Statistical tools can be used for better analysis of recorded result
  • Graphical presentation can be provided for better presentation of recorded result
  • Integration with SAP can be done so that approved result can be fetched directly from LIMS in SAP which can remove manual entry in SAP.
  • Use of AI for various analysis of trend for OOS or OOT can be made

Return on Investment

  • Management of QC sample and result (tracking, reporting, review and approval)
  • Cost effective and user friendly
  • Time saving as all result can be available online in one place (to take further decision on batch disposition)