Quality assurance
Last updated: 21 September 2026
1. Purity and batch-testing standards
Novex Peptide supplies UK research-use peptides to a ≥99% purity standard, with every batch tested before release.
2. Independent batch testing
Independent COAs are available in our Testing Documents library. Review each report for the tested substance, strength, batch and laboratory findings. Supplier test reports are clearly identified as supplier reference documentation and do not establish a match to Novex stock unless a batch match is documented.
3. Purity standards
Product specifications vary by compound and batch and are stated on the relevant product page. Where independent analytical results are available, they are displayed separately from manufacturer or supplier specifications. Manufacturer specifications and independently measured laboratory results are identified separately.
4. Evidence by product and batch
Read the actual report for the named product, strength and batch. A report for another batch does not verify the batch supplied.
5. Specifications and measurements
Supplier specifications describe the intended specification. Analytical results describe only the tested sample and method. HPLC area purity does not by itself establish vial mass, identity, sterility, endotoxin levels, clinical safety or efficacy. Those claims require their own suitable evidence.
6. Publication controls
Sample, demonstration, archived and unpublished records are excluded from the public report library. Published reports must identify the batch, provider, test date and document. Laboratory accreditation and independence are not inferred merely from a provider name.
7. Authenticity and limitations
Check a laboratory verification link or contact the issuing laboratory where possible. A hosted PDF alone is not independent authentication. Any discrepancy in batch, strength, label or document should be raised before ordering or handling.
8. Storage, traceability and release
Storage and transport requirements depend on the particular material and its supported documentation. Product release requires applicable supplier, batch, safety and transport records.
9. Research use only
Analytical documentation does not authorise human or animal administration, treatment, consumption or cosmetic use. Regulatory classification and supplier obligations remain product-specific.