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SOP 23 Quality Management System for the NIH Human Research Protection Program (HRPP)
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Document Date: 2014-03-10 08:07:14


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Company

HRPP / QA/QI / Scientific Counselors / /

Facility

Clinical Center / /

IndustryTerm

work products / clinical research protocol / human subjects protocols / individual research protocols / annual audit / organizational systems / /

MedicalTreatment

clinical research protocol / /

Organization

Intramural Clinical Research Steering Committee / NIH Fellows Committee / National Institute of Health / Clinical Center Department of Clinical Bioethics / QUALITY ASSURANCE PROFESSIONALS ADVISORY COMMITTEE / International Rugby Board / Clinical Center’s office of Protocol Services / office of Human Subjects Research Protections / Medical Executive Committee / IRB / Human Subjects Research Advisory Committee / FDA / NIH QI / FDA GCP / IRB Professional Administrators Committee / NIH HRPP / Association for the Accreditation of Human Research Protections Programs / Clinical Center / Research Steering Committee / /

Person

P. Annually / /

Position

Investigator / THE INSTITUTIONAL OFFICIAL / QI Officer / Director / THE QI OFFICER The QI Officer / the Deputy Director for Intramural Clinical Research / the Deputy Director for Clinical Research / the Chief / Chair / the Deputy Director for Intramural Research / Clinical Director / REQUIREMENTS The Institutional Official / Director for tracking purposes / officer / THE QI OFFICER / Quality Officer / Institutes and Centers / /

ProvinceOrState

Quebec / /

Technology

K. Updates technology / specific clinical research protocol / individual research protocols / research protocol / human subjects protocols / /

SocialTag