Abiozen operates an open, U.S.-based quality control platform offering independent analytical testingβwithout requiring marketplace purchasing or vendor dependency. Request verification directly and receive secure, digital Certificates of Analysis with rapid turnaround.
We operate as an independent quality authority. This separation reinforces neutrality, objectivity, and trust in every result we deliver.
Core Capabilities
We operate as an independent quality authority within the global life sciences ecosystem. This separation reinforces neutrality, objectivity, and trust in every result we deliver.
Open access testing available to all organizations worldwide.
24-48 hour digital Certificate of Analysis (CoA) turnaround.
Complete documentation, raw data access, and full audit trails.
cGMP, FDA, and ISO alignment with audit-ready systems.
Comprehensive testing for research, development, and quality assurance applications.
Receive comprehensive, digitally signed CoA documentation typically within 24-48 hours of sample receipt.
Delivered through secure portals with role-based access, version history, and audit trails.
Our quality control services are powerful on their own β but become truly exceptional when integrated directly into the Abiozen LLC platform. This creates a smooth, efficient, fully traceable workflow from product discovery to final quality verification.
Start quality control requests instantly while browsing products.
Secure API flow of certificates and batch info β zero manual re-keying.
Quick answers to the most common questions about our quality control and testing services.
No. Our quality control services are completely independent and available to all organizations. There is no requirement to purchase products through our scientific marketplace to access testing services.
Most chemical analysis and physical characterization tests have a 24-48 hour turnaround from sample receipt. Microbiological testing typically requires 3-7 days. Rush services are available for urgent needs.
We provide comprehensive digital Certificates of Analysis that include complete test results, method details, instrument information, reviewer/approver signatures, and compliance statements. All documentation is delivered through secure client portals.
Yes, our U.S.-based laboratory operates under cGMP principles with appropriate quality systems, documentation practices, and audit trails. We maintain compliance with FDA expectations and international quality standards.
We implement full ALCOA+ compliance across all operations, including electronic signatures, audit trails, version control, and data verification processes. All instruments are qualified and methods are validated according to regulatory requirements.
Yes, we have controlled storage facilities for temperature-sensitive materials. Please contact us for specific storage and shipping requirements for your samples.
Access reliable, third-party analytical testing with rapid turnaround timesβcompletely independent of marketplace activity.