Menu Back to Clinical-Trial-Fundamentals

Clinical Trial Fundamentals eLearning Program

Clinical Trial Fundamentals eLearning Program (all three modules!)

This program is designed to provide a practical context to help clinical research professionals learn about conducting clinical trials. Using an interactive case study with realistic scenarios designed to illustrate the learning points, the program follows the activities of a fictitious clinical investigator and their staff as they prepare for, initiate and conduct a clinical study. As learners make decisions during the clinical trial, the program illustrates how clinical trial regulations and guidelines impact each situation, and the complex details of clinical trial study management.

The online program includes three self-paced modules that can be accessed anytime, anywhere for one year. Continuing education credits are offered.

Add Program to Cart

*This ICH E6 R2 GCP Investigator Site Training meets the Minimum Criteria for ICH GCP Investigator Site Personnel Training identified by TransCelerate BioPharma Inc. as necessary to enable mutual recognition of GCP training among trial sponsors.

Explore the Program, Watch a Short Video!

Module 1 - Clinical Trials: Study Preparation

Featured Topics:

  • Responsibilities of the investigator and sponsor
  • Study documents and Study Design
  • Clinical trial phases
  • Use of placebo
  • International Conference on Harmonisation
  • Drug Development Legislation
  • Ethical considerations in clinical research
  • Responsibilities of the study staff
  • The site evaluation visit
  • The study budget and contract
Add Module 1 to Cart

Module 2 - Clinical Trials: Study Initiation

Featured Topics:

  • FDA Form 1572
  • Financial disclosure
  • Institutional Review Board
  • Informed consent and HIPAA
  • Study initiation documents
  • The investigator meeting and the study initiation meeting
  • Investigator study files
Add Module 2 to Cart

Module 3 - Clinical Trials: Conducting the Study

Featured Topics:

  • Subject recruitment, selection, retention, and compliance
  • Applying the informed consent process during a clinical trial
  • Classifying, recording, and reporting adverse events
  • Managing monitoring visits
  • FDA inspections
  • Post-study critique and study closure
Add Module 3 to Cart

Other DIA eLearning you may be interested in:

Informed Consent: Comprehensive Concepts and Components

Featured Topics:

  • Determining When Informed Consent Is Necessary
  • Comprehension Guidelines
  • Overview of Elements of Consent
  • Proper use of electronic consent, its benefits, and concerns with its use
  • Long Form versus Short Form, and Tips for Administering Consent
  • Changes to Informed Consent Under HIPAA
Add to Cart

Clinical Trial Management Comprehensive eLearning Bundle

This eLearning bundle includes the Clinical Trial Fundamentals eLearning Program and the Informed Consent: Comprehensive Concepts and Components module.

Add to Cart

Good Clinical Practice

Gain the basic knowledge required to conduct clinical trials, including information about subject safety, regulations, and the practicalities of performing clinical research studies. This module includes information about the recently adopted ICH GCP E6(R2) guideline. Learn through an interactive case study, knowledge checks, and flashcards.

Featured Topics:

  • GCP, Roles, Terms, and Origins
  • GCP Requirements, Regulations, Guidances and History
  • The Role of the Investigator
  • The Role of the Study Staff, sponsor and IRB
  • Aspects of GCP : Informed Consent; Adverse Event Handling and Reporting
Add to Cart

Digital Learning Catalog

DIA Learning: eLearning Soultions