Independent Quality Control Without Barriers.

Abiozen operates an open, U.S.-based quality control platform offering independent analytical testing—without requiring marketplace purchasing or vendor dependency. Request verification directly and receive secure, digital Certificates of Analysis with rapid turnaround.

24-48h Rapid
Turnaround
U.S. Based
Facility
Digital
CoA

The Abiozen Advantage

We operate as an independent quality authority. This separation reinforces neutrality, objectivity, and trust in every result we deliver.

Core Capabilities

  • Independent analytical testing
  • 24–48 hour turnaround
  • Digital CoA delivery
  • Full sample traceability
  • Secure storage & access
Our Differentiator

Quality Without Barriers

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.

Independence

Open access testing available to all organizations worldwide.

Speed

24-48 hour digital Certificate of Analysis (CoA) turnaround.

Transparency

Complete documentation, raw data access, and full audit trails.

Compliance

cGMP, FDA, and ISO alignment with audit-ready systems.

ALCOA+ Data Integrity

Lab Capabilities

  • cGMP-compliant laboratory operations
  • 21 CFR Part 11 electronic records
  • Qualified equipment & validated methods
  • Full ALCOA+ data integrity principles

Analytical Testing Services

Comprehensive testing for research, development, and quality assurance applications.

Chemical Analysis

  • Identity (FTIR, NMR, MS)
  • Purity (HPLC, GC)
  • Impurity Profiling
  • Residual Solvents
  • Elemental (ICP-MS)
24-48h TAT USP / EP / ICH

Physical Characterization

  • Particle Size Distribution
  • X-ray Diffraction (XRD)
  • Thermal (DSC, TGA)
  • Microscopy (SEM, TEM)
  • Surface Area (BET)
48-72h TAT ISO Standards

Microbiological

  • Sterility Testing
  • Endotoxin (LAL)
  • Microbial Limits
  • Bioburden Assessment
  • Preservative Effect
3-7 Day TAT ISO 11737
24-48 Hours

Digital Certificate of Analysis

Receive comprehensive, digitally signed CoA documentation typically within 24-48 hours of sample receipt.

  • Electronic signatures for authenticity
  • Complete results with acceptance criteria
  • Method references and instrument details
Secure Document Access

Delivered through secure portals with role-based access, version history, and audit trails.

Serving Diverse Industries

Pharmaceuticals
Biotechnology
Medical Devices
Academic Research
CDMOs / CROs
Agri-Chemicals
Cosmetics
Personal Care
Platform Integration

Seamless Platform Integration

Our quality control services are powerful on their own — but become truly exceptional when integrated directly into the Abiozen Scientific platform. This creates a smooth, efficient, fully traceable workflow from product discovery to final quality verification.

Direct sample submission

Start quality control requests instantly while browsing products.

Automated data transfer

Secure API flow of certificates and batch info — zero manual re-keying.

Platform Integration Flow

Frequently Asked Questions

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.

Analytical Services

Ready for Independent Quality Verification?

Access reliable, third-party analytical testing with rapid turnaround times—completely independent of marketplace activity.

Open to all organizations
Compliant documentation
Request Testing Services
Fast Response No Obligation Quote Secure & Confidential