Quality Assurance & Testing
Our rigorous QA process ensures every batch meets the highest purity and safety standards through independent third-party testing.
Our Quality Assurance Process
Raw Material Verification
All raw materials are sourced from certified suppliers and verified for authenticity before use in production.
Batch Synthesis
Production follows strict protocols with continuous monitoring. Each batch is assigned a unique tracking number.
Initial Testing
In-house preliminary testing for purity and safety. Multiple test points throughout the synthesis process.
Independent Lab Analysis
Samples sent to accredited third-party laboratories for comprehensive HPLC and NMR analysis.
Documentation
Complete Certificates of Analysis generated including test results, methodology, and batch information.
Release & Delivery
Only batches meeting 99%+ purity standards are released. COA included with every shipment.
HPLC Analysis
High Performance Liquid Chromatography determines purity levels and detects impurities. Results verify compound identity and concentration.
NMR Spectroscopy
Nuclear Magnetic Resonance confirms molecular structure. Detailed analysis validates chemical composition and integrity.
Gas Chromatography
GC/MS analysis identifies volatile compounds and traces. Detects contaminants down to parts per million.
Compliance & Certifications
ISO 17025
Our testing partners are ISO/IEC 17025 accredited for competence in testing and calibration.
GLP Standards
Good Laboratory Practice compliance ensures data integrity and quality across all testing procedures.
Research Use Only
All compounds certified for research use. Full documentation of restrictions and safety requirements included.
Batch Traceability
Complete traceability from raw materials through synthesis, testing, and delivery. Full audit trail available.
Testing Independence
Third-party testing ensures unbiased results. Laboratories selected for reputation and expertise.
Quality Records
Complete quality records maintained for 7 years. Available for institutional audits and compliance verification.
Certificates & COAs
Every batch comes with a complete Certificate of Analysis (COA) and documentation. Download samples and understand what's included.
Certificate of Analysis
Complete COA for each batch including HPLC, NMR, and GC/MS results. Shows purity percentage, impurities detected, and testing methodology.
View Sample COA →Test Report Bundle
Full technical reports from all testing methodologies. Detailed graphs, spectra, and analytical data for your records and institutional requirements.
View Sample Report →Batch Verification
Batch tracking document confirming product identity, manufacturing date, expiration date, and storage recommendations.
View Sample Verification →📋 Sample Certificate of Analysis
Batch Number
FM-2024-00542
Analysis Date
2024-12-15
Expiration Date
2025-12-15
Testing Laboratory
AccredLab Analytics
Test Results Summary
Methodology
- High Performance Liquid Chromatography (HPLC)
- Nuclear Magnetic Resonance (NMR) Spectroscopy
- Gas Chromatography-Mass Spectrometry (GC/MS)
- Karl Fischer Coulometric Titration (Water Content)
Storage & Stability
- Store at 2-8°C in dark, sealed containers
- Stable for 12 months under recommended conditions
- Protect from light and moisture
- Do not freeze
Testing Laboratory Information
- ISO/IEC 17025 Accredited
- GLP Compliant Testing
- Independent Third-Party Analysis
- Full Data Integrity Audit Trail
Third-Party Testing
All batches are tested by independent, accredited laboratories. Transparent testing ensures unbiased quality verification and absolute integrity.
Why Independent Testing?
We believe in radical transparency. Third-party testing eliminates any conflict of interest and provides you with absolutely unbiased analysis. Our testing partners are ISO/IEC 17025 accredited and follow GLP standards, ensuring the highest quality data integrity. Every batch results are available to you, documented, and verifiable.
HPLC Analysis
High Performance Liquid Chromatography separates and analyzes compound components. Determines purity percentage and detects any impurities or byproducts down to 0.1%.
NMR Spectroscopy
Nuclear Magnetic Resonance confirms molecular structure and composition. Validates that the compound matches the expected chemical structure precisely.
GC/MS Analysis
Gas Chromatography-Mass Spectrometry identifies volatile components and residual solvents. Detects trace contaminants at parts-per-million levels.
Our Testing Standards
ISO 17025
International accreditation for testing and calibration competence
GLP Compliant
Good Laboratory Practice standards ensure data integrity
Chain of Custody
Complete traceability from collection to analysis
Full Documentation
Complete records for audit and verification purposes
Quality Assurance
Regular internal and external quality checks
Timely Analysis
Fast turnaround without compromising accuracy
Our Testing Laboratory Partners
Leading provider of HPLC and NMR analysis services. 20+ years of experience in pharmaceutical and research compound analysis.
ISO 17025 AccreditedSpecializes in GC/MS and trace analysis. Advanced instrumentation for detecting contaminants at ppb levels.
GLP CertifiedMulti-technique testing facility with expertise in structural confirmation and purity analysis for research compounds.
ISO 17025 Accredited