The detail behind
every specification.
Request the documentation for the product and batch you are considering. A meaningful review connects identity, analytical results, test methods and the lot number.
From the product name
to the batch record.
Our team handles requests for certificates of analysis, identity testing, purity results and other relevant batch records. Specify the product, lot number if known, and any required tests in your enquiry.
- 01Match the material
Product name, molecular identity, batch identifier and sample details.
- 02Read the method
Test technique, acceptance criteria and the result for that sample.
- 03Verify the issuer
Report issuer, testing date and any applicable accreditation scope.
What laboratory reports
can tell you.
Analytical purity, peptide content and microbiological quality are distinct characteristics.
| Attribute | Typical approach | What to look for |
|---|---|---|
| Identity | Mass spectrometry and complementary methods | Evidence matching the named molecule, with sequence or structural detail where needed. |
| Chromatographic purity | HPLC or another defined separation method | Method conditions and component profile. A purity percentage is not automatically a content assay. |
| Content & composition | Appropriate quantitative assay | The measured material and amount. Each blend component needs its own specification. |
| Microbiological attributes | Applicable microbiological and endotoxin methods | Separate tests appropriate to the product; HPLC does not measure sterility. |
| Other quality attributes | Method-specific testing | Relevant residual solvents, water content, container or stability specifications. |
Documentation that matches
your research requirements.
Australia
Include any laboratory-accreditation requirements in your enquiry. Australian laboratory scopes can be checked through NATA.
NATA directoryCanada
Request the relevant test reports and issuer details for the selected material and intended research application.
Batch-specific reviewUnited States
Distinguish laboratory test results from FDA authorisation of a particular medicine or device.
Product-specific documentationLaboratory accreditation applies to a defined scope of activity. It is not a blanket approval of a supplier, every tested product or a therapeutic use. Directory links are verification resources, not claims of an Aurelis affiliation.
Read more about quality standards
Connect with Aurelis
Your next enquiry
starts with the details.
Tell us the compound, listed content, preferred presentation and destination. Our team can discuss local availability and the documentation for your selected material.