Experience and vision

DxTerity's leadership has extensive experience in advancing cutting-edge technology that redefines healthcare.

What drives us

Patient-first

At-home collection, simple workflows, and actionable results.

Scientific rigor

Peer-reviewed research and clinical validation at every step.

Access & equity

Removing geographic barriers to quality diagnostics.

Robert Terbrueggen, PhD

CEO and Founder

20+ years in genomics. Inventor of DxDirect Technology. Previously Director of R&D at Clinical Micro Sensors, Director of Research for Motorola Life Sciences. 26 issued US patents, 100+ international patents. PhD Chemistry from Caltech.

James Healy, MS

CFO and SVP Business Development

25 years of operations and financial leadership. Co-founded DxTerity Diagnostics with Bob. Cofounded JTA Research (acquired by Cadence). SVP for Cadence Design in Business Development. Previously CFO and SVP business development at Magnify360 a marketing automation firm. CFO and COO Hughes communication products. leading $250M+ in new business in high speed communication infrastructure.

Aviva Jacobs, PhD, PMP

VP, Product Development

20 years in IVD industry. Led FDA clearance of genetic tests for Warfarin, cystic fibrosis, and thrombophilia at GenMark Diagnostics. Oversaw BARDA-funded radiation exposure test development. PhD Genetics from George Washington University.

CAP Accreditation

CAP: 8680553, AU-ID: 1664134

College of American Pathologists accreditation ensuring the highest standards of laboratory testing quality.

CLIA Certificate

05D2054007

Certificate of Accreditation under the Clinical Laboratory Improvement Amendments program.

ISO 13485:2016

ISO Certificate

International standard for quality management systems in medical device manufacturing and design.

California State License

CDF-00343579

State of California Department of Public Health clinical laboratory license.

FDA EUA Authorization

EUA202120 (Granted 8/28/2020)

Emergency Use Authorization for the DxTerity SARS-CoV-2 RT-PCR CE Test.

New York State License

NY9654

New York State Department of Health Clinical Laboratory Permit.

Maryland State License

MD: Non-Expiring

Maryland Departmnet of Health Office of Healh Care Quality Clinical Laboratory Permit

Rhode Island State License

LCO01761

State of Rhode Island Department of Health Center for Health Facilities Regulations.

Pennsylvania State License

PA: 36662

Pennsylvania Department of Health Clinical Laboratory Permit.

2006

Founded

50+

US patents

12+

Publications

1M+

Tests processed

Compliance commitment

CAP-accredited, CLIA lab tests and IVD are run in accordance with applicable federal, state, and local regulations.

Contact Us

Stay in the know.

Get the latest updates and news.

DxTerity’s patient-focused mission is to bring the power of at-home RNA-based genomic monitoring to improve the management of immune-mediated diseases and overall patient well-being.

Products

Development Services

Technology

News

Contact us

Experience and vision

DxTerity's leadership has extensive experience in advancing cutting-edge technology that redefines healthcare.

What drives us

Patient-first

At-home collection, simple workflows, and actionable results.

Scientific rigor

Peer-reviewed research and clinical validation at every step.

Access & equity

Removing geographic barriers to quality diagnostics.

Robert Terbrueggen, PhD

CEO and Founder

20+ years in genomics. Inventor of DxDirect Technology. Previously Director of R&D at Clinical Micro Sensors, Director of Research for Motorola Life Sciences. 26 issued US patents, 100+ international patents. PhD Chemistry from Caltech.

James Healy, MS

CFO and SVP Business Development

25 years of operations and financial leadership. Co-founded DxTerity Diagnostics with Bob. Cofounded JTA Research (acquired by Cadence). SVP for Cadence Design in Business Development. Previously CFO and SVP business development at Magnify360 a marketing automation firm. CFO and COO Hughes communication products. leading $250M+ in new business in high speed communication infrastructure.

Aviva Jacobs, PhD, PMP

VP, Product Development

20 years in IVD industry. Led FDA clearance of genetic tests for Warfarin, cystic fibrosis, and thrombophilia at GenMark Diagnostics. Oversaw BARDA-funded radiation exposure test development. PhD Genetics from George Washington University.

CAP Accreditation

CAP: 8680553, AU-ID: 1664134

College of American Pathologists accreditation ensuring the highest standards of laboratory testing quality.

CLIA Certificate

05D2054007

Certificate of Accreditation under the Clinical Laboratory Improvement Amendments program.

ISO 13485:2016

ISO Certificate

International standard for quality management systems in medical device manufacturing and design.

California State License

CDF-00343579

State of California Department of Public Health clinical laboratory license.

FDA EUA Authorization

EUA202120 (Granted 8/28/2020)

Emergency Use Authorization for the DxTerity SARS-CoV-2 RT-PCR CE Test.

New York State License

NY: 9654

New York State Department of Health Clinical Laboratory Permit.

Maryland State License

MD: Non Expiring

Maryland Department of Health Office of Health Care Quality Clinical Laboratory Permit.

Rhode Island State License

License Number: LCO01761

State of Rhode Island Department of Health Center for Health Facilities Regulations.

Pennsylvania State License

PA: 36662

Pennsylvania Department of Health Clinical Laboratory Permit.

2006

Founded

50+

US patents

12+

Publications

1M+

Tests processed

Compliance commitment

CAP-accredited, CLIA lab tests and IVD are run in accordance with applicable federal, state, and local regulations.

Contact Us

Stay in the know.

Get the latest updates and news.

DxTerity’s patient-focused mission is to bring the power of at-home RNA-based genomic monitoring to improve the management of immune-mediated diseases and overall patient well-being.