Content
Data protection and the GDPR affects all companies. There are particularly strict requirements when sensitive patient data is processed. In light of the considerable risk of liability or fines, behavior that complies with data protection regulations is essential. The seminar provides a practice-oriented overview of the legal and organizational requirements and challenges and shows options for implementing data protection.
Many questions arise within the company:
- Should a data protection officer be appointed?
- Under what conditions may data from suppliers, customers, patients, etc. be processed?
- Can data be passed on within a group of companies?
- How should GDPR compliance be documented?
- What special features need to be taken into account when conducting clinical studies?
- How can information obligations be fulfilled?
- What threatens violations?
Topic overview
- Overview of the legal framework
- Data protection organization and data protection management
- Lawfulness of processing personal data (including health data)
- Roles in data protection law – (joint) responsibility and order processing
- Special features when conducting clinical studies (distribution of responsibility, need for regulation)
- Information obligations and other rights of those affected
- Data protection supervision, sanctions and claims of those affected
target group
Management and board of directors, in-house lawyers, data protection officers, managers and employees of manufacturers, dealers and importers of medical devices.
Prior knowledge
Not required.
Early bird discount
If you register up to 3 weeks before the start of the seminar, you will receive an early bird discount of 10 percent.
KONTAKT:
Online
