Choosing an experienced Contract Research Organization (CRO) will significantly reduce the risk of delays associated with your clinical trial. Nor Consult, LLC, will diligently support you, your vendors, sites and other key stakeholders to minimize the time between protocol completion and First Subject In (FSI).
As a full-service CRO, Nor Consult, LLC, assures in-depth knowledge in therapeutic areas associated with the spine and spinal cord, as well as orthopedics and obesity.
Understanding the unique regulatory process associated with medical device approvals is essential to moving your trial from concept to approval. At Nor Consult, LLC, we are proud to have an experienced team with specialized knowledge in the clinical and regulatory processes that are needed to safely and effectively manage medical device trials.