Implementing GDPR in your Organisation – eLearning

Reasons to attend

On the 25th of May 2018, the EU General Data Protection Regulation (GDPR) came into effect. But do you know what it means to your organisation and what impact it is on your day-to-day activities?

The GDPR does not only apply to EU organisations, but to all organisations worldwide, from the moment they have sensitive data from an EU citizen. Per definition, the impact on the pharma industry is huge since it uses personal data on a regular basis.

This implementing GDPR course will help you to put in practice the GDPR in a CRO/pharmaceutical industry.  

What's included?

• Documents and materials related to this course are included
• Globally recognised certificates awarded after test completion
• This course has been certified by TransCelerate and BioPharma
• This course has been reviewed by the Belgian GCP Inspectorate.

Course schedule

• Course credit: 6h (3 months period to complete course)
• Complete the course at anytime, anywhere!

Course Description

This eLearning course will explain how the GDPR affects your organisation, with focus on clinical operations but also for your business development activities, contracts with sites & vendors, etc.

Indeed, the organisation of clinical trials might also result in 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 data protection rules.

The purpose of the 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.

Once you completed the eLearning course, you will be offered to attend a live 1-hour webinar (1 session organised/quarter) with your trainer, Ms. Nancy Cottigny. Do not miss this opportunity to get all your questions answered by our subject matter expert.