Focused Expertise in Critical Therapeutic Areas
At Nor Consult, we specialize in high-stakes clinical trials across critical therapeutic areas, delivering outcomes regulators and payers demand.
Smart, flexible, and FDA-ready — our clinical research solutions are designed to deliver reliable results with precision, speed, and regulatory confidence.
Nor Consult is a specialized CRO and consulting partner supporting sponsors across devices, drugs, and combination products. From trial design to global approvals, our senior experts bring academic rigor, regulatory depth, and practical efficiency, helping sponsors achieve FDA- and EMA-ready data while minimizing risk and cost.
Guided by senior experts with decades of clinical, regulatory, and scientific experience, our leadership team ensures every project is designed and executed with precision.
I founded Nor Consult, LLC in 2005 with a clear vision: to bring rigorous science and practical wisdom together so that innovators in life sciences can deliver meaningful therapies to patients.
My career has been a journey through many roles, including professor, biostatistician, clinical epidemiologist, government advisor, and industry consultant. Each role gave me a different lens on the challenges of developing new therapies, and together they inspired me to create Nor Consult. My goal was to create a consultancy that brings together academic rigor and real-world experience, turning complex data into clear strategies that drive innovation and improve patient outcomes.
Two decades later, I’m proud of our collaborations with start-ups and global leaders alike, driving First-in-Human and pivotal studies, securing key regulatory approvals, and advancing therapies that change patients’ lives.
In addition to my role at Nor Consult, I serve as an emeritus faculty member at the University of Washington, where, since 1997, I have led research in clinical epidemiology, health outcomes, and medical product evaluation. This balance of academic leadership and hands-on industry work continues to shape our approach: scientifically grounded, results-driven, and always focused on patients.
Patrick Heagerty, PhD, is a Professor, former Chair of Biostatistics and Director of the Center for Biomedical Statistics at the University of Washington. He is nationally recognized for his deep expertise in clinical trial design and advanced statistical methodologies. Nor Consult has a multi-year partnership with Dr. Heagerty supporting our clients across various therapeutic areas, including medical device and cardiovascular trials.
His leadership roles, including on the FDA Sentinel Innovation Center, highlight his profound understanding of regulatory requirements and best practices in biostatistics. Dr. Heagerty’s guidance ensures robust study design, precise data analysis, and strategic insights crucial for successful clinical development programs.
Dr. Heagerty holds a BS in Biology from Cornell University, a MS in Statistics from State University of New York (Albany) and a PhD in Biostatistics from Johns Hopkins. He serves as a statistical editor for the Journal of the American Medical Association (JAMA) and is an elected member of the National Academy of Medicine.
At Nor Consult, we specialize in high-stakes clinical trials across critical therapeutic areas, delivering outcomes regulators and payers demand.
Partner with senior experts who deliver FDA- and EMA-ready data with efficiency and precision.
Meet Our Experts