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).
The list below shows some of the therapeutic areas and other research that the Nor Consult, LLC team has worked on.
Understanding the various regulatory processes associated with medical device and combination product approvals is essential to expeditiously moving your product to market. Nor Consult can assist you with: