Independent Verification Protocol
The research peptide industry has historically lacked transparency in quality verification. Purity claims often lack independent validation or public documentation.
Veritas requires every batch to undergo independent third-party testing using validated analytical methods. Results are published with unique batch identifiers, enabling researchers to verify authenticity before use.
Analytical Testing Methods
HPLC Analysis
High-Performance Liquid Chromatography
Quantifies peptide purity by separating compounds based on chemical properties. Provides precise measurement of target peptide concentration and identification of impurities.
Mass Spectrometry
Molecular Weight Verification
Confirms molecular identity by measuring mass-to-charge ratio. Detects structural modifications and verifies amino acid sequence integrity.
Dual Verification Protocol
Both HPLC and mass spectrometry analysis required for every batch. This dual approach provides:
- Quantitative purity measurement (HPLC) to verify concentration
- Molecular identity confirmation (MS) to validate correct structure
- Independent cross-validation using complementary analytical techniques
Complete Testing Pipeline
Synthesis
Peptides synthesized at verified partner facilities with documented synthesis and quality control procedures.
Initial Testing
In-house preliminary analysis to verify batch meets minimum standards before sending to independent lab.
Independent Lab Analysis
Third-party accredited laboratory conducts HPLC and mass spectrometry analysis on random sample.
Data Publication
Results published with unique batch ID. COA and testing data made publicly accessible.
Quality Verification
Internal review confirms ≥98% purity threshold. Batches below threshold are rejected.
Release for Distribution
Approved batches released with full documentation. Batch ID linked to all data.
Access complete testing documentation for any product using the batch verification tool.
Batch Verification Tool →