InfoLIMS for Laboratory

InfoLIMS has been the industry’s most technically advanced Laboratory Information Management System .

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InfoLIMS V1.0 useful project features

InfoLIMS has the most extensive and proven suite of Industry Best Practices in the Laboratory Information Management System industry.

Sample Request

Create sample testing request according to different sample specification, collection source, sample device and condition.

Parameters

InfoLIMS can manage all parameter related to Product Group, Sub Group & Matrix as per different discipline.

Testing & Verification

After approval request is assign to related tester and verifier as per role and department. Tester have to input data as per formula generated by form builder.

Quality Control

Quality manager select sample randomly from already generated request. It helps Measurement uncertainty provides information on the level of confidence on the measurement result

Audit Trail

Auditor check selected sample report with all parameter and test procedure. Auditor get raw data sheet generate by tester. And also check machine calibration report require for sample testing.

Machine Calibration

List of calibrate equipment, Calibration scheduler, History of calibration, history of repair, List of calibration agency as per equipment.

Stability

Stability testing is the process of testing samples over a period of time in order to determine how the material might be affected by storage under various conditions.

Inventory

Store Module allows the user to create product list and equipment use in the laboratory along with description. Track inventory, raise auto indent/generate indent, create purchase order and good received note as per purchase order.

Account & Billing

It helps to maintain financial transaction, set Parameter charges for billing, Generate Order/Bill, receipt of payment, generate quotation and maintain workorder as per client requirement.

HOW WE ARE DIFFERENT?

WORKFLOW

LIMS is a system designed to support public health, national reference laboratories, research laboratories or other non-clinical settings and are sample centric, with focus on data analysis and workflow and features to meet regulatory requirements.

  • Track laboratory information during the testing process (from sample log-in to reporting)
  • Collect, store, archive and analyze laboratory data
  • Report test results for patient care
  • Report data to administration, Ministry of Health (MOH) and other agencies

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