- About Us
An independent laboratory built around one question: what is actually in the vial?
- Mission
Clarity through analysis, not marketing claims
- Testing philosophy
Report the measurement, not the story
- Quality Control
A controlled path for every sample
Intake and chain of custody
Samples are logged against the submission form with condition, seal state and lot marking recorded on receipt.
Method assignment
Each test is assigned a documented SOP with a defined reference standard and system suitability criteria.
Analysis and calibration checks
Instruments are calibrated and verified before each run; calibration and sequence records are retained with the data.
Independent data review
A second qualified analyst reviews the chromatograms, calculations and limits before release.
Certificate issue and publication
The signed COA is issued and published to public verification under an immutable report number.
- Laboratory Standards
Instrumentation, documentation and retention
Instrumentation
RP-HPLC with UV-DAD detection, LC-MS for identity confirmation, ICP-MS for elemental impurities and kinetic chromogenic LAL for endotoxin.
Documented SOPs
Written procedures for sample handling, preparation, analysis, review and reporting, with analyst qualification records.
Reference standards
Certified standards used for identity confirmation and quantitative calibration, with lot traceability.
Record retention
Raw data, chromatograms and certificates retained under controlled access with immutable report identifiers.