Independent batch testing
Additional box, random selection at the shipper, laboratory analysis and a shipment hold. Release only after SYNOVA reviews and accepts the result.
QUALITY & DOCUMENTATION
Quality management.
Evidence you can review.
Independent laboratory batch testing is included with every order. From the additional box and random selection at the shipper to the shipment hold and release decision, SYNOVA manages the quality process.
Discuss testing requirementsA report in your brand name
Customer- or brand-name reporting with a QR code and verification code. This upgrades the report; the batch testing is already included.
Discuss the reporting upgradeSTANDARD · INCLUDED WITH EVERY ORDER
Every batch tested.
Every release reviewed.
Every order includes an additional box for testing. A box is selected at random at the shipper, and the shipment stays on hold until the independent laboratory result is available and accepted by SYNOVA.
A report applies to the sample and analytical scope it identifies. It does not establish results for untested products or parameters.
Raw-material documentation
Review the raw-material CoA against the agreed product requirements.
Production & sample preparation
Produce the order plus an additional box for batch testing, without reducing the customer’s confirmed quantity.
Independent sample selection
A box is selected at random from the finished order at the shipping partner and sent to the independent laboratory.
Laboratory testing
The independent laboratory tests the selected batch sample. The remaining shipment stays on hold at the shipping partner while results are pending.
Review & release decision
SYNOVA reviews the laboratory result and authorizes release only after acceptance. Pending or unresolved results keep the shipment on hold.
RESULTS ACCEPTABLE
Release & dispatch
After Synova’s review and release confirmation.
RESULTS UNRESOLVED
Keep on hold
Review and resolve before customer dispatch.
DOCUMENTATION FOR YOUR PROGRAMME
Review the right record
for the right question.
Confirm which documentation is relevant to your product, sample and agreed scope.
Raw-material CoA
Starting material identity and the available analytical documentation.
Finished-product report
The tested sample, product and batch, analytical methods and reported results.
Customer-name reporting · paid option
Optional, for an additional fee: the report is issued in the customer or brand name. Arrange the details before sample submission.
QR & verification codes · paid option
The optional customer-name report includes a QR code and verification code for checking the laboratory report.
DEFINED RESPONSIBILITIES
Clear roles at every stage.
Independent analysis and Synova oversight have different roles in the testing route.
Synova
Reviews raw-material documentation, coordinates production and sampling, reviews test reports and makes the shipment release decision.
Shipping partner
Receives finished goods, selects a box at random and sends it to the laboratory. Holds the customer shipment and dispatches it only after SYNOVA authorizes release.
Independent laboratory
Analyses the submitted sample against the agreed panel and issues the report identifying the sample, methods and results.
PEPTIDE PURITY & BATCH REPORTS
>99% Purity.
Batch-specific evidence.
Our general peptide purity specification is >99%. Product pages identify the references to which it applies.
What does the purity specification cover?
The specification describes the peptide purity requirement. The laboratory report records the measured result for its identified sample and analytical method. A general specification does not replace a batch-specific result.
How do I request a CoA?
Share the product name, reference specification and batch or order details, if available. We confirm which certificate of analysis (CoA), finished-product report and manufacturing records are available for your programme.
Is a report in my brand name included?
Independent batch testing is included with every order. Issuing the report in your customer or brand name, with QR and verification codes, is an optional upgrade for an additional fee.
DOCUMENTATION REQUEST
Bring your requirements
to the review.
Send the product, intended research application and documentation requirements.
Request the relevant raw-material records, finished-product testing scope and available manufacturing documentation. Facility-specific certificates and analytical requirements are reviewed for the actual supply programme.
Prepare a documentation requestLET’S BUILD YOUR PRODUCTION PROGRAMME
Your next production run.
Let’s plan it together.
Tell us what you want to produce, how you want it branded and where it needs to go. We’ll review the scope and requirements with you.