The Layered Links Model: An Alternative Approach to International Privacy Regulation
In: 10 International Data Privacy Law 253
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In: 10 International Data Privacy Law 253
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Working paper
In: (2018) 16:2 Canadian Journal of Law and Technology 307-338
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Working paper
In: In: Belinda Bennett and Ian Freckelton (eds), Pandemics, Public Health Emergencies and Government Powers: Perspectives on Australian Law (Federation Press, 2021), 165-180
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In: Garrett A. Johnson (forthcoming) Economic research on privacy regulation: Lessons from the GDPR and beyond in The Economics of Privacy, ed. Avi Goldfarb & Catherine Tucker. University of Chicago Press.
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A letter report issued by the General Accounting Office with an abstract that begins "The Department of Health and Human Services issued a final regulation in December 2000 that established rights for patients with respect to the use of their medical records. The regulation requires that most providers obtain patient consent to use or disclose health information before engaging in treatment, payment, or health care operations. The privacy regulation's consent requirement will be more of a departure from current practice for some providers than for others. Most health care providers, with the exception of pharmacists, obtain some type of consent from patients to release information to insurers for payment purposes. The new requirement obligates most providers to obtain consent before they can use and disclose patient information. It also broadens the scope of consent to include treatment and a range of health care management activities. Supporters of the requirement believe that the process of signing a consent form provides an opportunity to inform and focus patients on their privacy rights. Others, however, are skeptical and assert that most patients will simply sign the form with little thought. In addition, provider and other organizations interviewed are concerned that the new consent requirement poses implementation difficulties. They contend that it could cause delays in filling prescriptions for patients who do not have written consents on file with their pharmacies, impede the ability of hospitals to obtain patient information prior to admission, hamper efforts to assess health care quality by precluding the use of patient records from years past, and increase administrative burdens on providers."
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In: The Progress & Freedom Foundation Progress Snapshot, Band 6, Heft 1
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In: Privacy and Technologies of Identity, S. 239-253
In: CESifo Working Paper No. 10928
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This thesis will compare and discuss the different data privacy regulations found in the United States, China, and the European Union.
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Working paper
In: CEPR Discussion Paper No. DP16901
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In: Management Science
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In: International journal of information management, Band 76, S. 102753
ISSN: 0268-4012
In: OMEGA-D-23-00925
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