Mastering Good Clinical Practice A Comprehensive Training

Mastering Good Clinical Practice A Comprehensive Training
Last updated 3/2025
MP4 | Video: h264, 1920×1080 | Audio: AAC, 44.1 KHz

GCP

What you’ll learn

Core principles and international guidelines of Good Clinical Practice (ICH-GCP)

Ethical considerations and regulatory requirements in clinical research

Effective site management, monitoring, and auditing practices

Best practices for data integrity, documentation, and risk management

Compliance strategies to prevent common GCP violations

Requirements

This course is ideal for clinical research professionals, including investigators, study coordinators, monitors, regulatory affairs specialists, quality assurance professionals, auditors, and anyone involved in the design, conduct, monitoring, and reporting of clinical trials.

Description

Overview

Section 1: Introduction

Lecture 1 Introduction

Section 2: Core principles and international guidelines of Good Clinical Practice (ICH-GCP)

Lecture 2 Core principles and international guidelines of Good Clinical Practice (ICH-GCP)

Section 3: Ethical considerations and regulatory requirements in clinical research

Lecture 3 Ethical considerations and regulatory requirements in clinical research

Section 4: Effective site management, monitoring, and auditing practices

Lecture 4 Effective site management, monitoring, and auditing practices.

Section 5: Best practices for data integrity, documentation, and risk management

Lecture 5 Best practices for data integrity, documentation, and risk management

Section 6: Compliance strategies to prevent common GCP violations

Lecture 6 Compliance strategies to prevent common GCP violations

This course is ideal for clinical research professionals, including investigators, study coordinators, monitors, regulatory affairs specialists, quality assurance professionals, auditors, and anyone involved in the design, conduct, monitoring, and reporting of clinical trials.