DocumentationHow to Read a Certificate of Analysis (COA)
What each section of a research peptide certificate of analysis tells you, and how to match it to the vial on your bench.
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DocumentationWhat each section of a research peptide certificate of analysis tells you, and how to match it to the vial on your bench.
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Quality systemsThe documents to request, questions to ask and red flags to watch for when qualifying a research peptide supplier.
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Analytical methodsWhat reference standards are and how HPLC system suitability checks such as resolution, tailing, plate count and repeatability make results trustworthy.
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Lab safetyGeneral principles for segregating, labeling and accumulating lab chemical waste, and why your institutional EHS office and local rules have the final word.
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Quality systemsHow lot numbers connect a vial to its packing slip, COA and production records, and how labs and suppliers use traceability when issues arise.
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Contaminant testingWhy solvents can remain after peptide synthesis, how headspace gas chromatography measures them, and how ICH Q3C classes are used.
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Analytical methodsA practical walk through the ICH Q2(R2) validation characteristics and how to interpret “validated method” on a certificate of analysis.
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Contaminant testingBioburden, sterility and endotoxin answer three different microbiological questions. Here is what USP <61>, <71> and <85> each measure.
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DocumentationWhat each ALCOA+ principle means in practice, with paper and electronic examples, audit trail basics and a checklist for research labs.
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Contaminant testingHow USP <232>/<233> and ICH Q3D shape elemental impurities testing, how ICP-MS and ICP-OES compare, and how to read element results on a COA.
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Contaminant testingWhat endotoxins are, why they matter in cell-based research, and how gel-clot, turbidimetric and chromogenic LAL assays measure them.
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Analytical methodsHow tandem mass spectrometry reads a peptide sequence from b and y fragment ions, how peptide mapping works, and what MS/MS can and cannot distinguish.
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