AKESOgen is a CLIA-compliant laboratory with processes and procedures built around Good Clinical Practice, Good Laboratory Practice and the EU Clinical Trials Directive. We continually seek additional accreditations as part of our commitment to have a dynamic and constantly improving organization. We are involved and engaged with organizations promoting best practices and industry standards.

AKESOgen’s Quality Management Program is the foundation of our services and provides a uniform, unbiased quality assurance and control program. Whether you require our services to support your clinical trial or you need a CLIA compliant partner, AKESOgen has the expertise to provide results in compliance with all applicable regulatory requirements.

Our new laboratories are well-organized and spacious with the latest equipment and well-trained staff led by an experienced team of genomics scientists.

AKESOgen is adept at managing unique requests and we will ensure that whatever your project requires, it will be performed in compliance with appropriate authorities.

We invite and encourage our prospective customers to visit our facility to see first-hand how we can support your project. We have successfully been audited by leading healthcare companies and from this we have strengthened our partnerships and collaborations.

Components of our Quality Management Program include (but are not limited to):

  • External/ Customer Audit Hosting
  • Internal Audit Program
  • Proficiency Testing / Alternate Assessment Program
  • Business Continuity Planning
  • Disaster Recovery Policy
  • Incident Management and CAPA Planning
  • Equipment Monitors and Quality Control
  • Training

Click here to access HCP Fact Sheet

Click here to access Patient Fact Sheet

For additional information please contact us at


CLIA compliant: 11D2050537


Georgia License: 067-063


California License: COS 00800535

Florida License: 800027707

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