HIPAA Training for Clinical Trial Professionals
HIPAA Training for Clinical Trial Professionals
To purchase access for your team, or if you have any questions, email us at info@clinicalpathwaysresearch.com.
Course outline HERE
INTERACTIVE DEMO AVAILABLE BELOW
HIPAA's requirements for the use and disclosure of Protected Health Information (PHI) during the conduct of a clinical trial is not simple and depends on the situation. But there is a way to use a core set of principles and questions that provide an ability to manage and facilitate the needs of all stakeholders. The regulatory authority of HIPAA, the OCR and FDA agree that the two sets of regulations do not conflict and work well together. HIPAA does not restrict the GCP requirements of a site. Learn the answer to these questions and more in the eLearning course.
Did you know that not all clinical trial sites are covered entities?
How do you know if a clinical research site is a covered entity?
If a site is, do you know what they must do to follow HIPAA requirements to safeguard PHI?
Course Length: 60 minutes plus additional time for activities
INCLUDES:
Unlimited access to the content for 45 days from your initial day of purchase.
Certificate of completion
Extensive Case Studies
Post-Assessment
Knowledge Checks
LEARNING OBJECTIVES
Define key terminology and concepts specific to the HIPAA Privacy Rule in clinical research.
Describe when sites are covered entities and the sponsor roles and responsibilities related to the HIPAA Privacy Rule.
Discuss the requirements of the Privacy Rule relating to clinical research source documentation use and disclosure.
AUDIENCE
A foundation training applicable for all clinical research professionals involved with the conduct of clinical trials in the United States. This course includes extensive real-life case scenarios with review of example best answers.
INTERACTIVE DEMO:
