CaliberLIMS vs. LabVantage

Data integrity management in Chemical and microbiology laboratory. Paperless laboratory management. Online Data review. 21 CFR Par 11 compliance with date and time recordings, analyst tracking. Audit trial review. Sample management to track the testing and results, and pending sample status. Contemporaneous data entry. Reduce Human error. Online reconciliation of microbiological media details and other chemicals.

Probably better suited for true lab users. It is less suited for managing data requests. Most departments in our organization have abandoned allowing customers to enter their own requests because it is too complex and cumbersome.

Incentivized

• 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

• Worked very closely with us on developing the Statement of Work and provided us with a very good roadmap
• Programmers completed the changes and improvements on time.
• The contact for issues that arise on a daily bases is able to work with our people in a very professional basis.

Incentivized

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

• The currently LIMS system is web based. Unless you have java programmers on staff that can create new 'workflows', you will pay for the enhanced functionality

Incentivized

It is the best tools which is making life easy of the operators, analysts and microbiologist who are working in the chemical and microbiology laboratory. It is fully compliant with the regulatory requirement to adhere to the ALOCA++ principle, which gives confidence to the regulator to trust the data.

Easier sample management which includes sample tracking, sample analysis, results recording, results review and final COA for batch release. Audit trial management for data integrity compliance to meet the USFDA, EMA and other regulatory requirements. Audit trials enable ALOCA++ data integrity principles. Paperless system for resource management and time management in the Quality control laboratory.

We didn’t really have choice to use any other system. We probably would be able to better serve our customers with an issue tracking or help desk system.

Incentivized

• The system has freed up chemists' time and effectively helped us to grow 12% per year over the past 3 years without adding a chemist FTE

Incentivized