Showing results for IRB

Research Involving Pregnant Women, Fetuses, and Neonates
Discusses the historical exclusion of women of childbearing potential and the special requirements for conducting research involving pregnant women an...
Summit: Participant Recruitment and Retention
Recruiting and retaining participants comprise core components of clinical trials. The series describes methods for building trust with participants w...
Summit: Participant Recruitment
Learning Objectives: Describe best practices for identifying, recruiting, and motivating ideal potential participants. Explain IRB regulations...
On Tech Ethics Podcast - Ethical and Policy Issues for Xenotransplantation Clinical Trials
Season 1 - Episode 12 - Ethical and Policy Issues for Xenotransplantation Clinical Trials Karen Maschke, a Senior Research Scholar at The Hastings Ce...
Unanticipated Problems and Reporting Requirements in Social and Behavioral Research
Defines unanticipated problems, describes the reporting requirements associated with unanticipated problems, and identifies the types of actions an In...
Informed Consent and Incidental Findings in Research with Human Subjects
Defines incidental findings (IFs) in human subjects research and covers how IFs should be managed in the informed consent process. Provides an overvie...
Consent and Subject Recruitment Challenges: Therapeutic Misconception
Describes therapeutic misconception and identifies potential strategies researchers and institutional review board (IRB) members can use for reducing ...
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