Investigator Responsibilities - Safety Reporting For Investigational Drugs And Devices

Investigator Responsibilities - Safety Reporting for Investigational Drugs and Devices

U.S. Food and Drug Administration

Safety Reporting for Medical Device Studies - Responsibilities of the Investigators and Sponsor

GCP-Mindset - All About Clinical Research

Investigator Responsibility in FDA Regulated Research

The 12 Golden Rules of the Responsibilities of the Investigator

GCP-Mindset - All About Clinical Research

Investigational New Drug Safety Reporting Requirements (10of14) REdI 2018

U.S. Food and Drug Administration

Investigator Responsibilities The Good The Bad and The Ugly

Investigator Initiated Trials: Roles and Responsibilities Trailer

GCP for Investigators: Clinical Investigation Conduct and Reporting

WMDO

Safety monitoring in Clinical Trials - Responsibilities of the Investigators and Sponsor

GCP-Mindset - All About Clinical Research

Safety Reporting Requirements and Safety Assessment for IND and BA/BE Studies

U.S. Food and Drug Administration

Public Workshop: Safety Assessment for Investigational New Drug Reporting

Basic trainings for Investigators in Clinical Trials

GCP-Mindset - All About Clinical Research

FDA: Understanding the Role of the Food and Drug Administration - CountyOffice.org

You're in Charge: Principal Investigator Responsibilities

GCP Training and Clinical Trial Reporting: Impact on Investigators

Penn State CTSI

Clinical Investigator Training Course (CITC) Update - Operational Updates Part 1

U.S. Food and Drug Administration

Drugs & Devices in Research: An Introduction to Navigating FDA Oversight Requirements

UW Clinical Trials Institute

Decentralized Clinical Trials (DCT) Draft Guidance

U.S. Food and Drug Administration

PREVIEW - Safety Investigator & Investigation