The ECL standard
Every batch goes through manufacturer-commissioned independent testing, followed by a second round commissioned by East Coast Labs through Ozcanium Analytics. Both rounds must pass purity and bacterial endotoxin testing before release for sale.
Every batch.
Tested twice.
Our process at a glance · Research use only
Two independent rounds. Every batch.
Manufacturer-commissioned independent testing is our starting point. We commission a second round ourselves before a batch can be offered for sale.
Our manufacturer commissions independent laboratory testing of each batch. This first round covers purity and bacterial endotoxins, with the results documented in the manufacturer’s independent test reports.
We commission a separate round of independent testing through Ozcanium Analytics. Each batch is checked again for purity and bacterial endotoxins before we release stock for sale.
OUR RELEASE REQUIREMENT
Both rounds must pass purity and bacterial endotoxin testing before a batch is released for sale. If either round does not pass, that batch is not offered for sale.
An extra step, by choice
We value the manufacturer’s independent results. We also believe the responsibility to check should extend to us.
Commissioning our own testing gives every batch a second independent assessment before release. It is a deliberate part of how we work, because your trust deserves that care.
What those tests tell youUnderstand the result
Both testing rounds include purity and bacterial endotoxins. Here’s what each tells you, and how to read the result in context.
Explore analytical methodsHow much of the analytical signal is attributed to the target compound? The report gives the purity result under the stated method. Chromatographic peak-area purity and measured milligram content are different measurements.
A purity percentage is not a measurement of vial content.Are bacterial endotoxins present at a level the test can detect or measure? This separate analysis has its own method, units and reporting limits. The applicable report gives the result for the tested sample.
An endotoxin result does not establish sterility.Each must be read from its applicable tests. A purity percentage alone cannot establish all three. We publish the specific methods and results from each report.
Analytical results describe the tested sample and conditions. They do not establish suitability for human or animal use.
Care is part of our standard
Behind every order is someone placing their trust in us. We take that seriously. It shapes the testing we commission, the information we share and the way we answer your questions.
A batch must pass both independent testing rounds before we offer it for sale.
Clear records, honest context and help finding the certificate that applies to your supply.
An Australian team to help with product details, documentation and your order.
A closer look
A laboratory report should be something you can read and verify. Start with these five details.
The right record for your supply
Testing and online publication are separate. Every record is labelled so you can see exactly what it covers.
A reviewed certificate linked to the exact product size and stock lot. Your shipment’s allocated lot is identified separately during fulfilment.
An original report for the named supplier sample. It is not presented as the certificate for current ECL stock.
Our every-batch testing process still applies. Contact us for the document applicable to the supply you’re considering.
Let’s make it clear
Send us the compound, size and lot number if available.
Our team will help identify the applicable documentation.