ISO 17025 accredited analytical testing tailored for research peptides, custom sequences, and therapeutic peptide development
High-performance liquid chromatography (HPLC-UV/CAD) for accurate determination of peptide purity and related substance profiling. Custom method development available.
Typical turnaround: 3–5 days
High-resolution mass spectrometry for molecular weight verification, sequence confirmation, and structural characterization of research peptides.
Typical turnaround: 3–5 days
Comprehensive profiling of process impurities, deletion sequences, oxidation products, and other related substances using LC-MS and orthogonal techniques.
Typical turnaround: 4–6 days
GC-MS/MS analysis for residual organic solvents used in peptide synthesis, purification, and lyophilization processes.
Typical turnaround: 3–5 days
ICP-MS testing for elemental impurities in accordance with ICH Q3D guidelines. Ultra-low detection limits for research and regulatory support.
Typical turnaround: 4–6 days
Accelerated and stress testing to evaluate peptide stability, degradation pathways, and shelf-life under various conditions.
Custom protocols available
Development and validation of bespoke analytical methods for novel peptides, modified sequences, or unique impurity challenges.
Project-based pricing
Detailed, regulatory-ready CoAs with chromatograms, mass spectra, impurity tables, and full traceability for your research documentation.
Included with every test
Need a custom testing package or method development for your specific peptide?
Request a Custom Quote →