Maple
Laboratory Standards & Testing
Our commitment to quality assurance ensures that every research compound meets rigorous purity and identity standards before reaching your laboratory.
Our Quality Assurance Process
Third-Party Laboratory Testing
Tested batches are analysed by Testides, an independent third-party laboratory, using HPLC-UV at 214nm to verify purity and measured content against label claim.
Certificate of Analysis (COA)
Complete COA documentation available for each product, providing detailed analytical results including purity percentages, test methods used, and batch identification. These documents ensure full traceability for your research records.
Batch-Level Quality Control
Our quality control protocols are applied at the batch level, ensuring consistency across all units within a production run. Each tested batch is assigned a unique identifier for tracking throughout its lifecycle.
Validated Analytical Methods
Testing procedures follow established pharmacopeial methods and industry-standard protocols. Analytical validation includes specificity, accuracy, precision, and linearity assessments.
Purity & Testing Specifications
Minimum 99% purity for all peptide compounds
Endotoxin testing for applicable products
Heavy metal screening below detection limits
Microbial contamination testing
Moisture content analysis
Residual solvent verification
Documentation & Traceability
Each product shipped includes comprehensive documentation to support your research record-keeping requirements. Our batch management system maintains full traceability from synthesis through final quality release.
Certificates of Analysis are provided in PDF format and include the compound name, batch number, date of analysis, purity results, and testing laboratory identification. Additional documentation is available upon request for qualified research facilities.
Our quality management practices are designed to meet the documentation standards expected by research institutions and regulatory bodies for research-grade materials.
Related documentation: the analytical reports behind these standards are indexed on the Certificates of Analysis page, the methods used to generate them are explained in how peptide purity is verified, and guidance on reading a report line by line is set out in understanding COAs. Accreditation scope and what it does and does not cover is discussed in ISO 17025 accreditation scope on a peptide COA.
