HPLC Purity Analysis
Reverse-phase HPLC and UHPLC purity quantification for linear, cyclic, and modified peptides — impurity profiling to sub-0.1% detection, ICH Q3A compliant, UV/DAD detection.
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Verified Peptide & Bioanalytical Testing LaboratoryPeptide Testing & Bioanalytical Services
Peptide Testing & Bioanalytical Services
Verified. Precise. Delivered.
GLP-compliant HPLC purity testing, ESI-MS identification, sterility, endotoxin, and amino acid analysis for research and clinical supply. Every result delivered with a signed Certificate of Analysis.
Verified
Method Accuracy
500+
Compounds Tested
5–10
Business Day Standard TAT
CoA
Every Report, No Extra Cost
GLP-Compliant Testing ICH Q1A / Q3A Aligned Sterility Testing High-Resolution ESI-MS IND / DMF Ready CoA Arizona Pickup Available
Trusted By
Biopharma ResearchContract ManufacturingClinical Development
Our Testing Portfolio
One Standard of Excellence.
Every test performed with validated methodology and reviewed by expert analytical scientists. CoA included.
View All Services →Mass Spectrometry (ESI-MS)
High-resolution ESI-MS for sequence verification, PTM detection, disulfide mapping, and structural confirmation of peptides and modified analogs.
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Raw material and finished product identity confirmation for regulatory compliance, QC release, and lot-to-lot consistency — suitable for IND and DMF submissions.
Order This TestSterility Testing
GLP-compliant microorganism-free verification for injectable-grade peptides and research formulations. CoA-ready results.
Order This TestPotency Testing
Active ingredient strength and consistency verification for lot-to-lot reproducibility. Suitable for QC release and regulatory documentation.
Order This TestCustom Test Panels
Cyclic, PEGylated, stapled, phosphorylated, and D-amino acid peptides — tailored analytical programs for your compound type and regulatory context.
Contact For Pricing →Why Apollo Analytical
Built for Scientists Who Can't Afford Errors
CoA on Every Report
Signed, regulation-ready Certificate of Analysis with every test — suitable for IND, DMF, and US/EU regulatory filings. No upcharges.
5–10 Day Standard Turnaround
Standard turnaround of 5–10 business days. Rush 3–5 business day processing available. Optimized workflows without compromising data integrity.
Confidential & Secure
Compound data handled under strict confidentiality. Never shared with third parties. Signed agreements available on request.
Scientific Pre-Review
Every order undergoes scientific review by our laboratory team before analysis begins — ensuring optimal method selection, accuracy, and precision.
The Process
From Sample to Verified Report
A streamlined, rigorous process designed to minimize time-to-results at every step.
Submit Your Order
Complete our secure online form with sample details, test specs, compound type, and project context. We respond within 1 business day.
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🚗 Schedule a Pickup AZ OnlyShip or Drop Off
Receive detailed packaging, cold chain, and shipping instructions with your unique order reference. Arizona clients can use our complimentary pickup service.
Analysis Underway
Your sample is processed under strict QC oversight by credentialed analytical scientists. Track real-time status using your Order ID above.
Receive Your Verified Report
Your signed Certificate of Analysis and complete data package delivered securely to your inbox — regulatory-ready for IND, DMF, or QC release.
Ready to Submit Your First Order?
Secure, fast, and CoA-ready. Our team reviews every submission and responds within 1 business day.