Signed in as:
filler@godaddy.com
Signed in as:
filler@godaddy.com
Genomic MS is a healthcare consulting firm led by experts with over 20 years of clinical laboratory experience across hematology, clinical chemistry, immunoassay/serology, molecular diagnostics (PCR, sequencing), microbiology (bacteriology, mycology, parasitology), immunology, urinalysis, coagulation, blood banking/transfusion medicine, toxicology, cytogenetics, and pathology. We’ve partnered with laboratories, hospitals, and physician groups to improve compliance, accuracy, and operational excellence.
Genomic MS was founded with a clear vision: to bridge the gap between laboratory science and healthcare excellence. Our journey began more than 20 years ago when our founders worked in high-complexity clinical laboratories, gaining hands-on experience in hematology, chemistry, immunoassay, molecular diagnostics, microbiology, and immunology.
During the early 2000s, our team played a key role in laboratory setup, method validation, and instrument standardization for hospitals and private healthcare providers. By the mid-2010s, we expanded into training programs, quality management systems, and regulatory compliance consulting, helping laboratories achieve CLIA, COLA, CAP, and ISO 15189 accreditation.
At the height of the COVID-19 pandemic, our experts led critical initiatives in PCR testing, respiratory panels, and infectious disease diagnostics, supporting both public health and private laboratories with validations, workflow optimization, and rapid turnaround solutions.
Today, Genomic AMS stands as a trusted partner for laboratories worldwide, offering end-to-end consulting services—from new laboratory setup and staffing models to QC program development, CAPA/RCA training, and accreditation support. Our history reflects a consistent commitment to compliance, accuracy, and patient safety, and our future is focused on driving laboratories toward innovation and excellence.
We envision a world where every clinical laboratory, regardless of size, resources, or location, operates with the same commitment to quality, accuracy, and compliance.
In this vision:
We see laboratories worldwide meeting the requirements of CLIA, COLA, CAP, and ISO 15189, not just as obligations, but as opportunities to foster trust, elevate patient safety, and strengthen healthcare systems.
In this future, every test result—whether it comes from a hematology analyzer in a small rural lab or a high-throughput molecular PCR platform in a metropolitan hospital—carries the same weight of confidence, reliability, and integrity.
Our vision is built on the belief that patients everywhere deserve results they can trust, and that laboratories—when equipped with the right tools, training, and support—can become the cornerstone of safer, more effective healthcare.
Our mission is not only to consult, but to partner with laboratories—standing beside them as they grow, adapt, and excel in a rapidly evolving healthcare environment.
At Genomic MS, our mission is to empower healthcare providers and clinical laboratories with the knowledge, systems, and support they need to deliver accurate, reliable, and timely diagnostic testing.
We believe that every patient deserves results they can trust, and every laboratory deserves the tools and guidance to operate at the highest standards of quality and compliance. To achieve this, we are committed to:
We uphold the highest standards of honesty, transparency, and ethical practice in every aspect of laboratory consulting. Integrity means ensuring that laboratories not only meet regulatory requirements (CLIA, COLA, CAP, ISO 15189) but also operate beyond the minimum standards—building a culture of compliance that inspires confidence from regulators, providers, and patients alike.
Healthcare is rapidly evolving, and so must laboratory practices. We are committed to ongoing training and skill development for laboratory personnel, ensuring staff remain competent, confident, and inspection-ready. At the same time, we foster innovation by introducing cutting-edge diagnostic technologies, molecular testing platforms, and digital QC systems that increase accuracy, reduce turnaround times, and optimize workflows.
Modern laboratories generate enormous amounts of data—from QC results to patient trends. We transform this data into actionable insights, applying Westgard rules, Levey-Jennings analysis, method validation studies, and root cause analysis (RCA) to detect trends, prevent errors, and improve efficiency. By leveraging data analytics, we enable laboratories to make proactive decisions that enhance accuracy, reduce costs, and improve reliability.
Every service we deliver is rooted in the ultimate goal of improving patient care. We believe that behind every specimen is a patient whose diagnosis and treatment depend on the accuracy of laboratory results. By focusing on patient safety, reliability, and clinical value, we help laboratories become not just test providers but essential partners in patient health and wellness.
We use cookies to analyze website traffic and optimize your website experience. By accepting our use of cookies, your data will be aggregated with all other user data.