Care Access Training Academy

Basics of Clinical Research

Basics of Clinical Research training covers the basic concepts of clinical research. The course provides an overview defining what clinical research is and why it is necessary, how it differs from clinical care.

Adverse and Serious Adverse Event Reporting in Clinical Research Trials

This course aims to provide participants with the essential knowledge and skills to identify, evaluate, and record Adverse and Serious Adverse Events while upholding the utmost care for participant safety and data integrity standards.

Study Design, Conduct, and Documentation

Dissecting the Components of a Protocol

This course covers details about study protocols, and what items research staff should understand prior to and throughout a clinical research trial (also referred to as a clinical study).

Regulatory and Ethical Compliance

ICH GCP E6(R2) -Good Clinical Practice Fundamentals

This ICH GCP E6 (R2) Training meets the Minimum Criteria identified by TransCelerate BioPharma, Inc. as necessary to enable mutual recognition of GCP training among trial sponsors.

Regulatory and Ethical Compliance

Good Documentation/ALCOA-C Fundamentals

This training aims to provide participants with a comprehensive understanding of Good Documentation Practices (GDP) and the ALCOAC principles in clinical research.

Regulatory and Ethical Compliance

HIPAA Information Privacy and Security Training Module

The HIPAA courses are designed to help ensure HIPAA compliance, quality assurance, and risk reduction. The courses cover the HIPAA Privacy Rule, Security Rule, HITECH Act.

Regulatory and Ethical Compliance

HRPP Human Research Participants Protection (HRPP)

Human Research Participants Protection covers the importance of demonstrating respect for research participants, which is reflected in the principles used to define ethical research and the regulations.

Study Design, Conduct, and Documentation

The Fundamentals of Obtaining Informed Consent

The "The Fundamentals of Obtaining Informed Consent" course is designed to equip research professionals with the knowledge necessary to ethically and effectively obtain informed consent from participants.