Pioneering Innovation
Problem. Solved.
Quantigen is Now Part of Versiti
In tandem with Quantigen's range of preclinical and clinical research review services, Versiti's specialty CRO provides comprehensive, flexible services that range from IRB review through central laboratory services, biologistics, project management and more to support your unique study needs through every phase.
Creating elegant solutions.
Quantigen specializes in sample-to-answer method development and validation across a broad array of applications. For more than a decade, we have leveraged our expertise in molecular biology, biotechnology, and regulatory oversight to design customized, cost-effective workflows for our clients in three core areas:
Basic & Preclinical Research
Biomarker Development & Validation
Sample Prep, Assay, Protocol Optimization
Product Comparison Testing
Bioproduction Quality Control
Clinical & Translational Research
Process & Method Development
Analytical/Medical Device Development
Clinical Trials Support
Regulatory Filings
Clinical Diagnostics
Infectious Disease
Medication Management (PGx)
Partners & Collaborators
Why work with Quantigen?
We’re founded on the principal of creating durable scientific partnerships, earned and maintained through the consistent delivery of high-quality workflow solutions, excellent data quality and personalized support.
With total commitment to solving your most challenging scientific problems, we invite you to discover more.
Join Our Team
Explore our current job postings and discover new ways to elevate your career and maximize your potential with Quantigen.
Accreditations & Certifications
Quantigen is certified by the Centers for Medicare and Medicaid Services (CLIA # 15D2076283) and accredited through the College of American Pathologists (CAP Certificate # 8070743).
We are approved for patient diagnostic testing in all fifty States, including specific offerings through the State of New York (PFI:9406) and California (State ID: CDS-00800560).
Quantigen also maintains ISO 15189:2012 accreditation by A2LA (Certificate # 4842.01), demonstrating our dedication to the highest standards of data quality.
Each member of our laboratory and management staff proudly earns certification in Good Laboratory Practice (GLP) and Good Clinical Practice (GCP) as part of their company training requirements.
Our accreditation standards and proficiency testing requirements ensure a steadfast commitment by each laboratory member to procedural uniformity, testing integrity, and reporting accuracy.
Contact Us Today
Whether it’s a question regarding our services or complex compliance inquiries, we’re here to listen.
News & Insights
Check out our thinking in action and recent publications.
