Passive consent for clinical research in the age of HIPAA. - Wikidata - wikimedia - TriplyDB

Passive consent for clinical research in the age of HIPAA.

Passive consent for clinical research in the age of HIPAA.

http://www.wikidata.org/entity/Q35688279

about

The Effect of the Vermont Diabetes Information System on Inpatient and Emergency Department Use: Results from a Randomized Trial The Vermont diabetes information system: a cluster randomized trial of a population based decision support system Ethical issues in using data from quality management programs.When is informed consent required in cluster randomized trials in health research?Ethical oversight in quality improvement and quality improvement research: new approaches to promote a learning health care system Ethical and regulatory issues of pragmatic cluster randomized trials in contemporary health systems.Phenotypic information in genomic variant databases enhances clinical care and research: the International Standards for Cytogenomic Arrays Consortium experience.Facilitating enrollment in a Cancer Registry through modified consent procedures: a pilot study.Need for a roadmap for development of a coordinated national registry programme.Systematic bias introduced by the informed consent process in a diagnostic research study.Presence of cancer cells in the periarterial tissues of patients with advanced gastric cancer.

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P2860

Passive consent for clinical research in the age of HIPAA.

http://www.wikidata.org/entity/Q35688279

description

2006 nî lūn-bûn

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2006年の論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年论文

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2006年论文

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Passive consent for clinical research in the age of HIPAA.

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Passive consent for clinical research in the age of HIPAA.

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Passive consent for clinical research in the age of HIPAA.

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Passive consent for clinical research in the age of HIPAA.

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J.1525-1497.2006.00339.X

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Journal of General Internal Medicine

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Passive consent for clinical research in the age of HIPAA

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Charles D MacLean

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P2860

Potential impact of the HIPAA privacy rule on data collection in a registry of patients with acute coronary syndrome.

Survey of informed consent for registration of congenital anomalies in Europe

Variations among Institutional Review Board reviews in a multisite health services research study.

Problematic variation in local institutional review of a multicenter genetic epidemiology study.

Health Insurance Portability Accountability Act (HIPAA) regulations: effect on medical record research.

The Vermont Diabetes Information System (VDIS): study design and subject recruitment for a cluster randomized trial of a decision support system in a regional sample of primary care practices.

Improving primary care for patients with chronic illness.

US privacy laws may curb access to medical data.

Improving primary care for patients with chronic illness: the chronic care model, Part 2.

Impracticability of informed consent in the Registry of the Canadian Stroke Network.

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j.1525-1497.2006.00339.x

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207-211

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Benjamin Littenberg

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informed consent

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