About SAGA
Built for researchers who can't afford to guess.
SAGA was founded after years of watching research teams lose months of work to inconsistent sourcing. Compounds that arrived mislabeled. Purity claims that couldn't be verified. Suppliers that disappeared after the sale. We built SAGA to be the supplier we wished existed — one that treats documentation as a core product, not an afterthought.
Every compound in our catalog is synthesized in-house, verified by independent third-party labs, and shipped with a Certificate of Analysis tied to the specific batch you receive. We serve academic institutions, independent researchers, and clinical laboratories across North America and Europe.
“Research-grade should mean exactly that. Not ‘probably close enough.’ Not ‘verified by the same lab that made it.’ Every batch we release carries documentation we'd stake our reputation on — because we do.”
— SAGA RESEARCH TEAM
How We Work
From raw material to your lab.
Raw Sourcing
Amino acids and reagents are procured from audited pharmaceutical-grade suppliers with full traceability documentation.
Solid-Phase Synthesis
Each peptide is assembled via SPPS in our GMP-certified facility under controlled temperature and atmospheric conditions.
HPLC Purification
Crude product is purified using preparative HPLC to achieve ≥99% purity, with all fractions logged by batch ID.
Third-Party Verification
An independent ISO-accredited laboratory performs mass spectrometry and purity confirmation before release approval.
CoA & Dispatch
A Certificate of Analysis specific to your batch is issued. Product ships with cold-chain packaging and batch tracking.
Verified
Certifications & documentation
Every claim on this page is verifiable. Below are the actual standards, accreditations, and policies that govern our operations. We publish these because we believe transparency isn't a feature — it's a minimum requirement.
Quality Management
ISO 9001:2015
Certified under scope of peptide synthesis and quality management systems. Annual surveillance audits conducted by Bureau Veritas.
Analytical Verification
HPLC + MS
Each batch undergoes reverse-phase HPLC and ESI-MS at an independent ISO/IEC 17025-accredited laboratory. Reports are retained for 7 years.
Manufacturing Standard
GMP-Aligned
Our facility follows Good Manufacturing Practice guidelines for research chemicals, including environmental monitoring, SOPs, and change control.
Batch Retention Policy
36 Months
Reference samples from every production batch are retained for 36 months post-dispatch and are available for re-testing on request.
Certificate of Analysis
Per Batch
CoAs are issued per batch — not per product. You receive documentation specific to the material you ordered, not a generic lot report.
Our Customers
Who we serve.
Academic Laboratories
University and institutional research teams studying metabolic, neurological, and regenerative mechanisms. We support peer-reviewed work with full documentation suitable for publication appendices.
Independent Researchers
Individual scientists and small research groups who need clinical-grade compounds without pharmaceutical procurement minimums. Orders start at single vials with no volume commitment.
Clinical Laboratories
Licensed diagnostic and clinical facilities conducting in-vitro studies. We work within standard procurement workflows and can provide supplier qualification documentation on request.
Questions about our process, sourcing, or documentation?
Our team includes biochemists and analytical chemists who can answer technical questions directly. We don't route support through scripts.