Testing Lab Services
Analytical services
Comprehensive analytical and research support for pharmaceutical development, clinical research and industrial applications — for small molecules, biologics, peptides and raw materials.
Raw Material Testing
Identity, purity, assay and content-uniformity testing of active ingredients and excipients using USP and EP compendial procedures.
- USP / EP monograph testing
- Identity & purity by HPLC/UPLC
- Residual solvents & water content
Biomolecule Characterization
Structural and analytical characterization of peptides, proteins, vaccines and other biologics.
- Peptide mapping & sequencing
- Intact & reduced mass analysis
- Vaccine component characterization
Study Sample Analysis
Quantitative analysis of small and large biomolecules across preclinical and clinical phases.
- LC-MS/MS quantitation
- Method development & validation
- PK/PD sample analysis
Stability Studies
ICH-compliant stability programs including forced degradation and shelf-life estimation.
- ICH Q1A–Q1F storage conditions
- Forced degradation studies
- Shelf-life & expiry modeling
Purity & Content Assay
Precise determination of purity percentage and content in milligrams for finished materials.
- Chromatographic purity
- Content / potency assay
- Impurity profiling
Endotoxin & Safety Testing
Bacterial endotoxin testing to defined thresholds for release and regulatory support.
- LAL endotoxin testing
- Threshold PASS/FAIL reporting
- Release-ready documentation
Need testing or a certificate?
Reach out to discuss your study, or verify an existing certificate by its COA code.