content
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, compliance with data protection regulations is essential. The seminar provides an overview of the regulations that have been in force since May 25th, 2018 and the previous experiences with their implementation in practice.
Many questions arise within the company: What should be taken into account with regard to employees? May data be passed on within a group of companies? How to document compliance with the GDPR? In relation to suppliers, customers, cooperation partners and those affected, the following must be examined: Under what conditions may their data be processed? What special features must be taken into account when conducting clinical studies? How can the far-reaching information requirements be met? What is the risk of violations and who are the relevant actors?
topic overview
- Overview of the legal framework
- Privacy principles and permissions
- Processing of sensitive (health) data
- Order processing: special features when conducting clinical studies (distribution of responsibility, need for regulation)
- information requirements
- data subject rights
- documentation requirements
- Employee data protection
- Position of competitors, associations and authorities
- sanctions
target group
Managing directors and board members, in-house lawyers/syndics, data protection officers, executives and employees of manufacturers, dealers and importers of medical devices.
previous knowledge
Not mandatory.
KONTAKT:
Online
