Services

Purity Testing for Peptides and Endocrine Compounds

Our comprehensive analytical services utilize state-of-the-art instrumentation and validated methods to deliver accurate, reliable results for research and pharmaceutical applications.

Analytical Methods

LC‑MS/MS

Liquid Chromatography-Mass Spectrometry for precise identification and quantification of compounds.

HPLC/UPLC

High-Performance and Ultra-High Performance Liquid Chromatography with UV detection.

Immunoassays

Highly specific antibody-based assays for sensitive detection of target molecules.

Testing Parameters

Identity Confirmation

LC‑MS mass spectrum analysis for molecular identification and structural confirmation.

Purity Analysis

HPLC with UV detection at 214 nm for comprehensive purity assessment.

Assay (Content)

HPLC quantitative analysis for accurate content determination.

Water Content

Karl Fischer titration for precise moisture content measurement.

Endotoxin Testing

LAL (Limulus Amebocyte Lysate) assay for bacterial endotoxin detection.

Heavy Metals

ICP‑MS analysis for trace metal content determination.

Microbial Limits

USP <61> testing for microbial contamination assessment.

Residual Solvents

GC‑MS per ICH Q3C guidelines for solvent residue analysis.

Use Cases

Research Validation Studies

Supporting research projects with reliable analytical data for publication and regulatory submissions.

Reference Standard Verification

Confirming the identity and purity of reference materials used in analytical methods.

Batch-to-Batch Comparability

Ensuring consistency across manufacturing batches through comprehensive testing.

Pharmaceutical Method Transfer

Supporting method validation and transfer activities for pharmaceutical development.

Regulatory Submission Support

Providing data packages that meet regulatory requirements for drug development.

Ready to Discuss Your Testing Needs?

Contact us to learn more about our services and how we can support your research or pharmaceutical development.

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