12/15/2020
Why Take a Course in The General Data Protection Regulation (GDPR) and Clinical Trials?
Clinical trials are increasingly global by nature. The GDPR may apply to your clinical trial if conducted in a country within the European Economic Area (EEA) or the United Kingdom (UK). The GDPR data protections are broad in nature but it makes it clear that protection of personal data includes data created during the course of a clinical trial. Understanding the role your organization plays, which data are personal, and what constitutes a valid consent under GDPR requirements is key to compliance. This course highlights how HIPAA differs from GDPR, including reporting of data breach and notice requirements.
Learning objectives:
Determine the importance of subject data protection related to the General Data Protection Regulation (GDPR).
Describe the process to collect and analyze private data and ensure its security under the GDPR.
Recognize potential impacts of the GDPR and how it affects your organization.
Tired of training that does not understand your needs? Clinical Pathways eLearning uses real-life case scenarios to help you understand how it applies to your day-to-day.
To sample an interactive demo or to purchase the full course, visit our store here.
Interested in more than one course or to build a curriculum for your team? Clinical Pathways also offers convenient course bundles at a discounted rate. Each course comes with a certificate of completion as evidence of your training for audit readiness.
Need to train your entire department? Clinical Pathways offers enterprise solutions that are scalable to your department needs, including white label solutions or creation of new content for your internal training.
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- The Clinical Pathways Team
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