Search results
Results from the WOW.Com Content Network
Data subjects must be informed of their privacy rights under the GDPR, including their right to revoke consent to data processing at any time, their right to view their personal data and access an overview of how it is being processed, their right to obtain a portable copy of the stored data, their right to erasure of their data under certain ...
Data from the PCEHR is to be predominantly used in patient healthcare, but other uses are possible, for policy, research, audit and public health purposes. The concern is that in the case of research, what is allowed goes beyond existing privacy legislation.
The main legislation over personal data privacy for the personal and private sector in Switzerland is the Swiss Federal Protection Act, specifically the Data Protection Act, a specific section under the Swiss Federal Protection Act. The Data Protection Act has been enacted since 1992 and is in charge of measuring the consent of sharing of ...
Get ready for a lobbying furor, because there’s suddenly a plausible, bipartisan, bicameral push to finally give the U.S. a comprehensive data-privacy law, going way beyond the protections for ...
Personal data, also known as personal information or personally identifiable information (PII), [1] [2] [3] is any information related to an identifiable person.. The abbreviation PII is widely used in the United States, but the phrase it abbreviates has four common variants based on personal or personally, and identifiable or identifying.
Such data has proved to be very valuable for researchers, particularly in health care. GDPR-compliant pseudonymization seeks to reduce the risk of re-identification through the use of separately kept "additional information". The approach is based on an expert evaluation of a dataset to designate some identifiers as "direct" and some as "indirect."
The GDPR requires anyone processing someone’s personal data (meaning any data that can be linked to them as an identifiable person) have a legal basis for doing so.
An early attempt to create rules around the use of information in the U.S. was the fair information practice guidelines developed by the Department for Health, Education and Welfare (HEW) (later renamed Department of Health & Human Services (HHS)), by a Special Advisory Committee on Automated Personal Data Systems, under the chairmanship of ...