Quality Center
Quality & Documentation
Transparency You Can Verify.
OligoPoly Laboratories publishes a defined release specification, per-lot analytical documentation, and lot traceability records so that research customers can evaluate what they are buying before they buy it.
Quality Philosophy
Precision, transparency, and documentation.
The foundation stays factual: published specifications, per-lot records, and documentation that can be checked against the product in hand.
Published specification
Acceptance criteria are published before release, not written after the fact to fit whatever a lot happens to measure.
Component-level labeling
Blends are labeled by the quantity of each component. Aggregate totals are a derived sum, never the primary claim.
Lot traceability
Every released lot carries a distinct identifier linking the supplier record, the laboratory accession, and the published COA.
No fabricated data
We do not create purity values, chromatograms, or laboratory results. If a figure is published, a laboratory produced it.
Release Specification
What a lot must meet before we release it.
These are the acceptance criteria every lot is measured against. They are published so that customers can check our documentation against our own stated standard rather than taking a marketing claim at face value.
| Criterion | Requirement | Method |
|---|---|---|
| Identity | Confirmed for every declared component | LC-MS |
| Purity | Reported per lot; figure and basis stated on the COA | HPLC-UV |
| Component content (blends) | Each declared component within ±15% of its labeled quantity | HPLC-UV against reference standard |
| Component content (single compounds) | Within ±15% of labeled quantity | HPLC-UV against reference standard |
| Appearance | Consistent with the documented product description | Visual inspection at receiving |
| Documentation | Third-party COA on file, reviewed and approved by someone other than the uploader | Quality review |
How blends are labeled
A blend is labeled by the quantity of each component, for example GHK-Cu 50 mg / KPV 10 mg / TB-500 10 mg / BPC-157 10 mg. Any aggregate figure shown alongside it is the arithmetic sum of those components and is not itself a specification.
When a lot is outside specification
A lot that falls outside ±15% on any component is recorded as a deviation at quality review. It is not released as a routine pass. The deviation, its investigation, and its outcome are documented, and where a lot has already been published the record appears in the public correction log.
Why ±15%
±15% reflects realistic manufacturing and analytical variability for research-grade multi-component blends. We publish the figure rather than leaving it undefined so that a deviation is a documented event rather than a judgement call made after the result arrives.
Documentation Standards
Every standard connected to a record path.
Documentation follows the material from receiving through laboratory analysis to release.
Incoming material is inspected, reconciled against supplier documentation, and assigned an OligoPoly lot identifier distinct from the supplier lot.
A sample is submitted to an accredited laboratory for identity and purity determination by HPLC and LC-MS.
Results are checked against the published release specification by a reviewer who did not upload them. Deviations are recorded before any release decision.
Only reviewed and approved lots are released, and their documentation is published against the lot identifier.
Documentation Without Compromise
Quality records should be visible, structured, and specific.
COA records, analytical context, and acceptance criteria are organized so that a buyer can evaluate a lot on evidence rather than on assurance.
- Acceptance criteria are published before lots are measured against them.
- Laboratory values appear only where a laboratory record supports them.
- Deviations are recorded and disclosed rather than quietly absorbed.
- Every published figure can be traced to a specific lot and accession number.
Documentation Hub
COA, batch, testing, and policy paths in one place.
Each card connects a quality question to the most relevant published documentation resource.
COA Library
Search available Certificates of Analysis by product and lot context.
Browse COAs →
Batch Verification
Start with batch lookup when you have a lot, SKU, or documentation question.
Verify Batch →
Testing Methods
Review analytical method context, purity terminology, and documentation boundaries.
View Methods →
Specifications
Use published documentation resources where available for product review.
Open Downloads →
Research Standards
Review intended-use boundaries and Research Use Only language.
View Policy →
Returns & Claims
Find policy and support pathways for order, documentation, and quality questions.
View Policy →Frequently Asked Questions
Quick answers. Clear boundaries.
Where can I find the COA for my lot?
Use the COA Library or Lot Verification with the lot identifier printed on your vial label. Documentation is published against the lot identifier, not the product name alone.
What tolerance do you hold components to?
Each declared component must fall within ±15% of its labeled quantity. A lot outside that range is recorded as a deviation at quality review rather than released as a routine pass.
Why do you label blends by component instead of total milligrams?
An aggregate figure tells you nothing about the ratio you are actually receiving. Component-level labeling states each quantity directly, and the total is simply their sum.
What does Research Use Only mean?
Research Use Only materials are laboratory compounds. They are not for human or veterinary use, and OligoPoly Laboratories does not provide dosing, administration, reconstitution, or personal-use guidance.
How is purity determined?
Purity is determined by third-party HPLC-UV, with identity confirmed by LC-MS. The purity figure and the basis on which it was calculated are stated on the certificate for each lot.
What happens if you publish something incorrect?
Corrections are recorded in a public correction log rather than edited silently. A published record that changes should show that it changed.
Validation Review
Verified. Documented. Traceable.
The items below describe documentation review pathways and quality-control practices. They are not third-party certifications and are not presented as such.
Secure & encrypted
Your data is protected.
Third-party testing
Records reviewed by lot.
Full traceability
Supplier record to release.
Disclosed deviations
Public correction log.
Research-use products are not for human consumption, diagnostic use, therapeutic use, veterinary use, or clinical application.
OligoPoly Laboratories does not provide dosing, administration, reconstitution, or personal-use guidance, and does not sell to individuals for personal use.