Independent analytical testing
Clear results.
Better decisions.
Defined analytical scope, documented sample handling, and direct reporting for research peptides, raw materials, supplements, cosmetic actives, and custom samples.
Sample received / scope review pending
Defined scope
before acceptance
Sample-level
documentation
Clear methods
and limitations
Digital reporting
for every project
What we evaluate
Testing built around
the question.
Select a focused analysis or request a custom testing plan. Method, sample quantity, timing, and reporting format are confirmed before shipment.
Peptide identity
Assess whether a submitted research sample is consistent with the named compound using the method confirmed in your scope.
Mass-spectrometry pathwayPurity profile
Separate the primary component from detectable related peaks and document the chromatographic profile under the agreed conditions.
Chromatography pathwayContent testing
Evaluate the measured amount of a target analyte using an agreed method, calibration approach, and suitable reference material.
Quantitative pathwayCustom matrices
Request a technical review for supplements, cosmetic actives, raw materials, finished products, or other research matrices.
Feasibility review firstSample categories
One intake.
Many matrices.
Tell us what the sample is, what you expect it to contain, and what the result needs to support. We confirm feasibility before material is shipped.
Research peptides
Lyophilized or supplied in an agreed research matrix
↗BSupplements
Capsules, powders, liquids, and finished formulations
↗CCosmetic actives
Raw actives and formulated cosmetic research samples
↗DRaw materials
Incoming ingredients, reference materials, and intermediates
↗ECustom projects
Feasibility review for nonstandard compounds and matrices
↗From question to report
A documented path
for every sample.
Communication begins before shipment and continues through final reporting. Nothing is accepted until the scope is understood.
Request an intake review ↗Define
Tell us what the sample is, what it is expected to contain, and the decision the result needs to support.
Scope
Receive written confirmation of the proposed analysis, sample quantity, price, timeline, and reporting format.
Ship
Use the assigned submission reference and packing instructions. Do not send material before acceptance.
Analyze
The agreed analytical pathway is performed and the resulting data is reviewed for report preparation.
Report
Receive a digital analytical report tied to the submitted sample and its unique accession number.
Illustrative document only. It is not an analytical result.
Built for traceability
Reporting that says
what was tested.
Each issued report identifies the sample, analysis, result, and relevant limitations. Supporting data and verification options depend on the project scope.
- Unique accession and sample identifiers
- Method and result summary
- Report date and review status
- Scope-specific notes and limitations
Before you submit
Common questions.
How much sample should I send?+
The required amount depends on the material, target analyte, matrix, method, and whether repeat or confirmatory work may be needed. Your written scope will state the accepted amount before shipment.
Do you accept materials other than peptides?+
Yes, feasibility reviews may be available for supplements, raw materials, cosmetic actives, formulated products, and custom research matrices. Acceptance is never automatic.
Will I receive a Certificate of Analysis?+
Your scope will identify the reporting format. A laboratory report or certificate may be issued when appropriate, but the document applies only to the sample received and the work actually performed.
How long does testing take?+
Turnaround begins after the sample is accepted and logged. Timing varies with method readiness, queue, sample condition, reference-material availability, and any agreed follow-up work.
Can I ship a sample immediately?+
No. Submit an intake request and wait for written acceptance, a submission reference, and packing instructions. Unapproved shipments may be rejected or disposed of under the sample-handling terms.