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Informed consent is a process for getting permission before conducting a healthcare intervention on a person. A health care provider may ask a patient to consent to receive therapy before providing it, or a clinical researcher may ask a research participant before enrolling that person into a clinical trial. -- Wikipedia

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This document explains the general conditions under which this practice sees patients. It does not constitute an informed consent to any specific treatment. Informed consent will be provided each time you visit the pract
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Privacy Without Monopoly: Data Protection and Interoperability | Elect

Update, June 11, 2021: Today, we updated this paper with a new appendix, The GDPR, Privacy and Monopoly, which analyzes the legal benefits of interoperability under the GDPR, where a regional privacy law creates a stur
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