Data protection in Clinical Research

 

Data protection in Clinical Research

Clinical Research Related Courses

The purpose of this half day course is to explain how and  under what conditions you can gather, collect, process, transfer (inside or outside the European Union), anonymise or encode and delete personal data as part of clinical trials.

Related Courses
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20 Jun 2012 Brussels English
550,00 €
  • Full description & trainer
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Full description

The organisation of clinical trials might also include important data protection issues. It is important to know under what conditions the personal data of the patients participating in clinical trials (and of the investigators) can be processed in accordance with the applicable European and Belgian data
protection rules. The purpose of this half-day course is to explain how and under what conditions you can gather, collect, process, transfer (inside or outside the European Union), anonymise or encode and delete personal data as part of clinical trials.

Who should attend?

Anyone working in Clinical Research who wishes to understand the Data Protection Laws and their implementation.

Trainers
  • Belgian and European data protection rules: definitions
  • The applicable obligations when processing and transferring personal data
  • How to apply the data protection rules in practice
  • To be able to identify the important data protection issues when organising clinical trials
  • To become confident with the applicable Belgian and European data protection regulations
  • To learn how to apply the data protection rules in practice