Data Protection for Investigators and Study staff

This course has been designed for investigators and their team managing personal health data who would like to understand their role in this European Regulation. In this e-learning, the important concept related to data protection are reviewed such as the difference between regular or sensitive data, or the distinction between identifiable data, pseudonymous data, and anonymous data. Then, the role and responsibility of the investigator and his team are explained; when they are involved in a clinical trial but also in their daily practice. The actions to take in case of data breach or subject request related to personal data is also reviewed. We explain the participant, they are also data subjects in some circumstances and the same rights apply to them. Finally, a few field situations are reviewed.

Beginner

LEARNING OBJECTIVES:

    1. Raise awareness of data protection for investigators and their team
    2. Understand how GDPR applies to clinical research and medical practice in hospital
    3. Know the role and responsibilities of investigators and their team

 

This course includes a final QUIZ and a personal Certificate of completion or knowledge

 

WHO SHOULD ATTEND?

Hospital employees who work with health data and needs to understand the basics of the GDPR. This course has been created specifically for those people because health data are considered sensitive data under the GDPR and should be protected with extra care. It is essential to understand how the European Regulation on Data Protection applies in order to know your role, take appropriate precautions, ensure that patient rights and security are respected.

 

Why take this course?

This course has been specifically designed by experienced Data Protection Officers and Clinical Research Professionals for investigators and their team managing personal health data who would like to understand their role in this European Regulation and its implementation

Program

Prerequisites

You don’t need any prerequisite to follow this course : Hospital employees can start this course from scratch and gain the necessary knowledge to keep the data safe!

How it works

You will start with the key concepts of the GDPR applied to clinical research and medical practice at the hospital, followed by how to apply them in the context of a clinical study or your daily practice, i.e. what to do and when to do it.

This course is a very practical training, composed of interactive questions and study cases.

Languages ​​available

English
You can contact us for a translation of this training

Duration

45min

Price

The prices of our trainings are decreasing according to the desired quantity

Audience

Nurse
Doctor
Clinical (ClinOps, Data Management, Biometrics Medical Writing, etc.)
Medical Affairs
R&D

Included

This course includes a final QUIZ and a personal Certificate

Why participate in this e-learning?

Autonomy

Continuous learning

Group prices

Certificate

Interactive experience

Developed by GDPR experts

Ready to take up the challenge?

Contact us for any group purchase request or additional questions about the different courses