The paper focuses on the role of informed consent to processing of genetic data in the current and multi-level legal framework. Firstly, it will seek to determine if it is possible to process genetic data even without any form of consent according to the GDPR. Then, it will show that accountability principle plays a key role not only in the GDPR, but also at international and national levels. Finally, the paper will point out that nowadays data processing can no longer be regarded as a private relationship between the controller and the data subject. In this context administrative fines imposed by the Data Protection Authority have to be added to the civil liability of the controller. Furthermore, it is recommended to add a preventive rem...
The collection and use of biological samples and data for genetic research, or for storage in a biob...
The General Data Protection Regulation (GDPR) sets a high bar for consent for the processing of pers...
This article focuses on whether a certain form of consent used by biobanks - open consent - is compa...
The paper focuses on the role of informed consent to processing of genetic data in the current and m...
Genetic data contain sensitive health and non-health-related information about the individuals and t...
Abstract Background Genetic databases are becoming in...
The necessity to develop collections of big health data concerning an increasing number of persons, ...
Owing to the unique qualities of genetic data, there have been numerous criticisms of the current da...
This article sheds a light on how the data protection requirements enshrined in the General Data Pro...
This Thesis evaluates the role of informed consent in biobank research and the impact of the General...
This article focuses on whether a certain form of consent used by biobanks - open consent - is compa...
What are the different steps you have to consider if you plan to share sensitive data (including hum...
Since the turn of the millennium biobanks – stores of biological samples and associated data for res...
The collection and use of biological samples and data for genetic research, or for storage in a biob...
Legal Protection and Ethical Management of Genetic Databases: Challenges of the European Process of...
The collection and use of biological samples and data for genetic research, or for storage in a biob...
The General Data Protection Regulation (GDPR) sets a high bar for consent for the processing of pers...
This article focuses on whether a certain form of consent used by biobanks - open consent - is compa...
The paper focuses on the role of informed consent to processing of genetic data in the current and m...
Genetic data contain sensitive health and non-health-related information about the individuals and t...
Abstract Background Genetic databases are becoming in...
The necessity to develop collections of big health data concerning an increasing number of persons, ...
Owing to the unique qualities of genetic data, there have been numerous criticisms of the current da...
This article sheds a light on how the data protection requirements enshrined in the General Data Pro...
This Thesis evaluates the role of informed consent in biobank research and the impact of the General...
This article focuses on whether a certain form of consent used by biobanks - open consent - is compa...
What are the different steps you have to consider if you plan to share sensitive data (including hum...
Since the turn of the millennium biobanks – stores of biological samples and associated data for res...
The collection and use of biological samples and data for genetic research, or for storage in a biob...
Legal Protection and Ethical Management of Genetic Databases: Challenges of the European Process of...
The collection and use of biological samples and data for genetic research, or for storage in a biob...
The General Data Protection Regulation (GDPR) sets a high bar for consent for the processing of pers...
This article focuses on whether a certain form of consent used by biobanks - open consent - is compa...