Clinical Research Monitoring for Sponsors & CRO

TRAINING PROGRAM

Course ID: CSR0021 Obtaining Approval for Clinical Trials in US & EU for Regulatory Professionals

Course ID: CSR0121 Clinical Trials and Drug Development 

Course ID: CSR0221 Clinical Trials: Preparation and Design 

Course ID: CSR0321 Clinical Trials: Preparing for an Audit or Inspection 

Course ID: CSR0421 Corrective and Preventive Action (CAPA) Process Planning for Clinical Research Professionals 

Course ID: CSR0521 CRO Oversight 

Course ID: CSR0621 Clinical Safety Data Management: Definitions and Standards for Expedited Reporting (ICH E2A) 

Course ID: CSR0721 Structure and Content of Clinical Study Reports (ICH E3)