Documentation is the AVODAGEN product. Built around independent accredited verification and the KORECOA batch certificate for qualified business account procurement. Research use only.
Each batch is delivered with a complete documentation set. The standard research-grade documentation package is described below. Custom pharmaceutical-grade development engagements include expanded documentation appropriate to the intended use, by request.
Full analytical Certificate of Analysis covering HPLC purity and identity, mass spectrometry confirmation, water content, endotoxin testing, and residual solvent analysis. Heavy metals and sterility testing available for vialed product.
Each batch carries a KORECOA batch certificate consolidating accredited laboratory results, processing records, and origin documentation into a single verifiable package with batch-level traceability and partner authentication.
Safety Data Sheet (SDS) with handling, hazard, storage, and transport information prepared to international format standards for each supplied material.
Technical data sheet covering molecular specification, storage conditions, reconstitution guidance, stability information, and handling instructions for research use.
Available in custom pharmaceutical-grade development engagements: documented supplier qualification including regulatory standing, inspection history, and quality systems verification supporting institutional and pharmacy board review.
Available in custom pharmaceutical-grade development engagements: Korean processing records and origin documentation under applicable customs and trade frameworks supporting documented chain of custody.
KORECOA is the verification and documentation platform AVODAGEN is building behind each batch. Analytical verification is structured to be performed by accredited Korean laboratory partnerships independent of the upstream supplier and the Korean processor. This third-party structure is the difference between supplier self-certification and accredited institutional verification.
Verification is performed by accredited Korean laboratories independent of both the upstream supplier and the Korean processor. Documentation does not rely on supplier self-certification alone.
Institutional and pharmaceutical buyers require analytical results from a party with no commercial interest in the material. Independent verification is the foundation of defensible documentation.
Analytical work is performed through ISO/IEC 17025 and KOLAS accredited Korean laboratory partners. Accreditation requires demonstrated technical competence, validated methods, traceable measurement standards, and ongoing third-party audit.
Accreditation is independent confirmation that the laboratory operates to international competence standards, not a self-declared quality claim.
Each KORECOA batch certificate links analytical results, processing records, and origin documentation to a single batch identifier with a verifiable audit trail accessible through partner authentication.
Procurement and compliance review require the ability to trace every claim back to its source documentation. Batch-level traceability makes the documentation auditable.
Each batch certificate is timestamped with an append-only audit trail, designed so that documentation cannot be silently altered after issue.
Documentation integrity over time is what allows a buyer to rely on a certificate months or years after the transaction, including under audit.
Standard analytical release panel performed per batch. Additional parameters are added by molecule and by customer requirement. Research-grade peptides are supplied at greater than 99 percent purity.
High-performance liquid chromatography for purity quantification and identity confirmation. Research-grade material supplied at greater than 99 percent purity.
Mass spectrometry confirmation of molecular weight and identity against expected specification.
Karl Fischer titration for water content determination supporting accurate net peptide content.
Bacterial endotoxin testing on aqueous and vialed products to documented thresholds.
Gas chromatography headspace analysis for residual solvent quantification against specification limits.
Heavy metals analysis and sterility testing available for vialed product and on customer requirement, extending the standard panel where the application requires it.
Each batch is accompanied by a downloadable validation packet: HPLC purity trace, ESI-MS identity confirmation, and the KORECOA batch certificate from accredited (ISO 17025 / KOLAS) analysis. Processing is performed at our Primary CDMO Partner Node under documented transfer. Sample packets are available to verified business accounts on request.
// Sample packet is representative and provided for evaluation. Batch-specific certificates are released to qualified business accounts following verification. Research use only. Not for human consumption or therapeutic use.
Qualified business accounts can request a documentation sample, sample material for evaluation, or bulk pricing for specific molecules and quantities. Business account verification is required before commercial documentation is shared.
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