Standards & Accreditation

Standards and accreditation are the frameworks that let a test result mean something beyond the laboratory that produced it. This pillar covers what ISO/IEC 17025 accreditation actually certifies, the USP and ICH chapters behind endotoxin, sterility, heavy-metal, and residual-solvent testing, and how a buyer can check a laboratory scope independently. Accreditation is always specific to a named method, never a blanket seal of quality.

Articles in this Pillar / 10

1. 001The Third-Party Peptide Testing Landscape Explainedlabowned editorial
2. 002ISO 17025 Explained: Why Lab Accreditation Matterslabowned editorial
3. 003The Australian Peptide Research Landscape for 2026labowned editorial
4. 004Ozcanium Analytics: Independent Testing in Australialabowned editorial
5. 005Endotoxin Testing Explained: LAL Method and USP 85labowned editorial
6. 006Sterility Testing (USP 71): What It Actually Proveslabowned editorial
7. 007Heavy Metals Testing for Peptides: ICP-MS & ICH Q3Dlabowned editorial
8. 008Residual Solvents Testing for Peptides: ICH Q3C Guidelabowned editorial
9. 009Amino Acid Analysis for Peptide Content: USP 1052 Explainedlabowned editorial
10. 010Synthetic Peptide Quality Attributes: USP 1503 and 1504 Explainedlabowned editorial

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