about
Innovating consent for pediatric HCT patientsHuman Subjects Protection and Technology in Prevention Science: Selected Opportunities and ChallengesTranslational Bioinformatics: Past, Present, and FutureImmortal Life of the Common Rule: Ethics, Consent, and the Future of Cancer ResearchDesign, rationale, and baseline characteristics of the randomized double-blind phase II clinical trial of ibudilast in progressive multiple sclerosisMeta Consent - A Flexible Solution to the Problem of Secondary Use of Health Data.Improving biobank consent comprehension: a national randomized survey to assess the effect of a simplified form and review/retest interventionBecoming partners, retaining autonomy: ethical considerations on the development of precision medicine.Toward precision medicine and health: Opportunities and challenges in allergic diseasesSociety for immunotherapy of cancer (SITC) statement on the proposed changes to the common ruleAn informatics research agenda to support precision medicine: seven key areasThe Quantified Brain: A Framework for Mobile Device-Based Assessment of Behavior and Neurological Function.Lessons from HeLa Cells: The Ethics and Policy of Biospecimens.Unravelling the human genome-phenome relationship using phenome-wide association studies.Public Trust in Health Information Sharing: A Measure of System Trust.An Assessment of the Human Subjects Protection Review Process for Exempt Research.Assessing Researcher Needs for a Virtual Biobank.Navigating the Institutional Review Board (IRB) Process for Pharmacy-Related Research.Biobanking Research and Privacy Laws in the United States.Understanding the links between privacy and public data sharing.Concise informed consent to increase data and biospecimen access may accelerate innovative Alzheimer's disease treatments.Standard Versus Simplified Consent Materials for Biobank Participation: Differences in Patient Knowledge and Trial Accrual.Recognizing Risk and Vulnerability in Research Ethics: Imagining the "What Ifs?"Glomerular Diseases: Registries and Clinical Trials.A checklist for clinical trials in rare disease: obstacles and anticipatory actions-lessons learned from the FOR-DMD trial.Stakeholder-driven, consensus development methods to design an ethical framework and guidelines for engaged research.
P2860
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P2860
description
2015 nî lūn-bûn
@nan
2015 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
name
Bringing the Common Rule into the 21st Century
@ast
Bringing the Common Rule into the 21st Century
@en
Bringing the Common Rule into the 21st Century
@nl
type
label
Bringing the Common Rule into the 21st Century
@ast
Bringing the Common Rule into the 21st Century
@en
Bringing the Common Rule into the 21st Century
@nl
prefLabel
Bringing the Common Rule into the 21st Century
@ast
Bringing the Common Rule into the 21st Century
@en
Bringing the Common Rule into the 21st Century
@nl
P2860
P3181
P356
P1476
Bringing the Common Rule into the 21st Century
@en
P2093
Kathy L Hudson
P2860
P304
P3181
P356
10.1056/NEJMP1512205
P407
P577
2015-12-10T00:00:00Z