Lubricant Quality Control

Laboratory Software Built for the Complexity of Lubricant Manufacturing

From base oil characterization to finished product release, BLISS gives lubricant labs the structure, traceability, and control you need.

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Comprehensive Solutions for Laboratory Data

Datacor Laboratory Solutions gives lab managers a connected suite of tools to manage samples, enforce SOPs, automate QC workflows, and maintain compliance records from a single platform.

BLISS LIMS

Sample management, quality data, and compliance.

BLISS SQC+

ASTM D6299 and EPA Part 1090-compliant SQC Workflow.

BLISS Instrument Pro

Direct instrument integration to eliminate manual data entry.

BLISS CAPA

Streamline CAPA workflows to resolve lab quality issues faster.

How We Help

BLISS gives contract laboratories the automation, traceability, and reporting tools needed to serve clients and maintain the data integrity your reputation depends on.

1. Test Library Complexity, Solved

BLISS structures even the most complex test libraries — supporting method speciation across hundreds of customer- and product-specific variations without redundancy or data loss.

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2. Full Traceability from Raw Material to Finished Product

BLISS maintains an unbroken chain of custody from base oil intake through blending and final product release, giving you the documentation trail your customers and auditors expect.

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3. One System for Every Spec

BLISS manages customer specs, internal grade requirements, and API/ASTM method standards simultaneously across your entire product portfolio, without juggling spreadsheets.

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4. COAs That Write Themselves

Generate accurate, formatted Certificates of Analysis directly from approved test results — eliminating manual compilation and the errors that come with it.

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5. Keep Your Measurement Systems in Control

SQC+ delivers ASTM D6299-compliant statistical quality control built for industrial labs — monitoring method performance and flagging instrument drift before it becomes a quality event.

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6. Close the Loop on Every Out-of-Spec Result

CAPA ties corrective and preventive action directly to OOS events — giving your quality system the documented, auditable workflow required for ISO/IEC 17025 and customer audits.

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