The BMA and the Law Society have produced a new consent form for patients to sign when asking, through a solicitor, for their medical records to be released. The form is designed to ensure that patients give informed consent to the disclosure of their records, amid concerns that patients ...
A Model for Expanded Public Health Reporting in the Context of HIPAA The advent of electronic medical records and health information exchange raise the possibility of expanding public health reporting to detect a broad range... S Soumitra,NS Calman,H George - 《Journal of the American Medical Inf...
There needs to be renewed debate about the automatic need for consent to review medical records where the chance of personal harm is negligible and the purpose of the review is to provide robust evidence to save lives, prevent needless suffering, and improve the effectiveness and efficiency of ...
; when research usesonly medical records; and ... Doyal,L. - 《Bmj British Medical Journal》 被引量: 363发表: 1997年 Informed consent: the intricacies: Should the BMJ reject all studies that do not include informed consent? Should the BMJ reject all studies that do not include informed ...
Patients' Release of Medical Records: Involuntary, Uninformed Consent? Background: Informed consent is a mainstay of clinical practice, with both moral and legal forces. Material disclosure about extreme treatments, however, i... KJ David,JL Holmes,A Judith - PS 被引量: 20发表: 1985年 加载...
i、That the monitor(s), the auditor(s), the IRB, and the regulatory authority(ies) will be granted direct access to the participant’s original medical records for verification of clinical trial procedures and/or data, without violating the confidentiality of the participant, to the extent ...
Ⅹ、Confidentiality of Personal Information 个人资料的保密 The consent document must state (ICH GCP 4.8.10): i、That the monitor(s), the auditor(s), the IRB, and the regulatory authority(ies) will be granted direct access to the participant’s original medical records for verification of cl...
A cell line is when cells are grown continuously in the lab, to provide samples for medical researchers to test. Sometimes the cell lines continue long after the patient herself is dead. One cell line has been kept going since the 1950's, for example. ...
evidence-based research required to inform policies and regulations, e.g., third-party payer prac- tices; encourage the development of companion diagnostics; integrate genomic data into both electronic medical records and clinical decision-support tools; and establish recommenda- tions for best ...
aDigital imager, all sizes 数字式印象,所有大小[translate] aRecurrent disease events and deaths will be ascertained from subjects’ medical records upon re-consent of the subjects. 周期性疾病事件和死亡从主题将被查明’病历在再同意主题。[translate]...