Suzanne M Rivera
Dados Biográficos
| ID | 6763397 |
|---|---|
| NOME | Suzanne M Rivera |
| PRENOMES | Suzanne M |
| SOBRENOME | Rivera |
| ASSINATURA | RIVERA S M |
| AFILIAÇÕES | Case Western Reserve University |
| ORCID | 0000-0003-0240-6429 |
| VERIFICADO | Sim |
| TOTAL DE OBRAS | 3 |
| TOTAL DE CITAÇÕES | 0 |
| OBRAS COMO AUTOR | 3 |
| OBRAS COMO EDITOR | 0 |
| PRIMEIRO ANO DE PUBLICAÇÃO | 2015 |
| ANO MAIS RECENTE DE PUBLICAÇÃO | 2020 |
| ÍNDICE H | 0 |
Academic Advocacy
Medical school faculty and their colleagues in schools of nursing, public health, social work, and elsewhere often research issues of critical importance to health and science policy. When academics engage with government policymakers to advocate for change based on their research, however, they may find themselves engaged in “lobbying,” thereby entering a complex environment of legal requirements and institutional policies that they may not full…
CTSA Institution Responses to Proposed Common Rule Changes
In 2015, the U.S. Department of Health and Human Services (HHS) and 15 other federal departments and agencies proposed revisions to the Federal Policy for the Protection of Human Subjects. In this Notice of Proposed Rulemaking (NPRM), the departments sought to strengthen, modernize, and make more effective human subjects regulations while reducing administrative burden, delay, and ambiguity. We reviewed public comments from National Institutes of…
Investigator Experiences and Attitudes About Research With Biospecimens
To advance scientific knowledge about human diseases and effective therapeutic treatments, investigators need access to human biospecimens and associated data. However, regulatory and procedural requirements may impede investigators' efforts to share biospecimens and data within and across institutions. Although a number of studies have explored experiences and attitudes of study participants and others about biospecimen and data sharing, less is…
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Investigator Experiences and Attitudes About Research With Biospecimens
To advance scientific knowledge about human diseases and effective therapeutic treatments, investigators need access to human biospecimens and associated data. However, regulatory and procedural requirements may impede investigators' efforts to share biospecimens and data within and across institutions. Although a number of studies have explored experiences and attitudes of study participants and others about biospecimen and data sharing, less is…
CTSA Institution Responses to Proposed Common Rule Changes
In 2015, the U.S. Department of Health and Human Services (HHS) and 15 other federal departments and agencies proposed revisions to the Federal Policy for the Protection of Human Subjects. In this Notice of Proposed Rulemaking (NPRM), the departments sought to strengthen, modernize, and make more effective human subjects regulations while reducing administrative burden, delay, and ambiguity. We reviewed public comments from National Institutes of…
Academic Advocacy
Medical school faculty and their colleagues in schools of nursing, public health, social work, and elsewhere often research issues of critical importance to health and science policy. When academics engage with government policymakers to advocate for change based on their research, however, they may find themselves engaged in “lobbying,” thereby entering a complex environment of legal requirements and institutional policies that they may not full…
Political science (3 obras) · Alternative medicine (2 obras) · Biomedical Ethics and Regulation (2 obras) · Engineering ethics (2 obras) · Ethics in Clinical Research (2 obras) · Health Systems, Economic Evaluations, Quality of Life (2 obras) · Human research (2 obras) · Informed consent (2 obras) · Law (2 obras) · Medicine (2 obras)