Regulatory Science Symposium: Monitoring and Auditing Session 3: Auditing GCP Systems for Data Integrity (2016)
In this series, we will discuss data integrity, GCP systems, regulatory framework enforcement, and auditing for data integrity
Regulatory Science Symposium: Monitoring and Auditing Session 2: FDA Inspections - Getting Ready (2016)
In this series, we will discuss regulatory complexities regarding clinical trials.
Regulatory Science Symposium: Monitoring and Auditing Session 1: Introduction to Monitoring, Auditing, and FDA Inspections & GCP (2016)
In this series, we will discuss regulatory complexities regarding clinical trials.
Regulatory Science Symposium: Clinical Trials Hurdles Session 5 - Clinical Trial Data Disposition, Results, and Transparency Group (2015)
In this series, we will discuss how to successfully support and manage clinical trials
Regulatory Science Symposium: Clinical Trials Hurdles Session 4 - Trial Master Files (2015)
In this series, we will discuss how to successfully support and manage clinical trials.
Regulatory Science Symposium: Clinical Trials Hurdles Session 3 - FDA GCP Inspections (2015)
In this series, we will discuss how the FDA investigators would conduct their GCP investigation.
Regulatory Science Symposium: Clinical Trials Hurdles Session 1 and 2 - Challenges of Clinical Trial Management (2015)
In this series, we will discuss how to successfully support and manage clinical trials.
Introduction to Clinical and Translational Research: Study Population and Study Design - Session 2
This course outlines basic concepts and terminology in the design of clinical/translational research projects targeting specific populations, and discusses methods to identify useful study populations within large and diverse cities. These online video…