NHRC has implemented Standard Operating Procedures and a Quality Assurance department that conducts weekly QC and ensures investigator and coordinator training. Our Regulatory Department ensures a 2-3 day turnaround time on regulatory documents and contracts. Our Standard of Practice of utilizing central IRBs ensures fast review and approval of our clinical trials.
Our focus remains on producing quality data as our source documents are all consistently organized across all trials. Additionally, we audit 100% of our informed consents, as well as all studies prior to close out.