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Course Outline

Introduction

Overview of Various Clinical Research Types and the Corresponding GCP Focus Areas

  • GCP for Clinical Trials with Investigational Drugs and Medical Devices (U.S. FDA-Based)
  • GCP for Clinical Investigations of Devices
  • GCP for Clinical Trials with Investigational Drugs and Biologics
  • (ICH-Based)
  • GCP for Social and Behavioral Clinical Research

Understanding Ethics and the Role of Institutional Review Boards (IRBs) in Clinical Trials and Research

Overview of the Role, Purpose, and Basic Requirements of the ICH E6 GCP Guidelines

Understanding the Distinction Between ICH GCP E6 and U.S. FDA Regulations

Understanding the Investigator's Role and Responsibilities in Clinical Trials

Understanding the Role and Responsibilities of Industry Sponsors in Clinical Trials Under an Investigational New Drug (IND) Application

Understanding Informed Consent Requirements and Methods for Obtaining and Documenting Consent

Implementing Privacy Policies and Ensuring Participant Confidentiality in Clinical Trials

Ensuring Participant Safety and Well-Being in Clinical Trials

Detecting, Evaluating, and Reporting Adverse Events in Clinical Trials

Conducting Data Quality Assurance and Ensuring Integrity in Clinical Research

Designing and Conducting Clinical Trial Protocols

Understanding the Importance of Protocol Compliance in Clinical Trials

Conducting Clear and Proper Documentation and Record-Keeping in Clinical Trials

Understanding and Preparing for Clinical Trial Audits and Inspections

Preventing Research Misconduct

Recruiting and Retaining Participants for Clinical Trials

Drafting and Negotiating the Clinical Trial Agreement (CTA)

Summary and Conclusion

Requirements

  • A college degree in any discipline
 21 Hours

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