Скачать или смотреть CITI Program Preview - Document Control and Study Documents

This series examines the details of Good Documentation Practices (GDP). The two courses describe the requirements for writing controlled documents and discuss practical ways of maintaining proper systems for managing study documents. The series outlines the role that essential documents play in Good Clinical Practice (GCP). It also details rigorous procedures for creating study documents and entering study data in Electronic Data Capture (EDC) systems.

Suggested Audiences: Clinical Research Associates (CRAs), Clinical Research Coordinators (CRCs), Contract Research Organizations (CROs), Faculty, Principal Investigators (PIs), Quality Control/Quality Management Professionals, Regulatory Affairs Professionals, Research Administrators, Sponsors, Study Sites

To learn more, please visit: https://about.citiprogram.org/series/...