×
Log in
Upload File
Most Popular
Study
Business
Design
Technology
Travel
Explore all categories
The top documents tagged [elements of informed]
FDA Compliance Actions Against IRBs and Clinical Investigators Paul W. Goebel, Jr., CIP Vice President
[email protected]
Chesapeake Research Review,
217 views
Wendy Lloyd BA, LPN, CIP,CCRP Regulatory Affairs and Compliance Specialist
224 views
Informed Consent Philosophy 2803 Lecture IV Feb. 5, 2003
213 views
BUILDING INFORMED CONSENT FOR PESTICIDE HANDLERS IN WASHINGTON Karl F. Weyrauch MD MPH Family Physician Research Consultant UW PNASH Member, Western Institutional
218 views
Informed consent
397 views
1 Choice and Autonomy Ethical Issues in Women’s Health Meredith Schwartz Dalhousie University, Department of Philosophy
212 views
Northeast Ethics Education Partnership (NEEP) Training Resources To access NEEP’s training materials, please visit
229 views
Ethical Principles for Biomedical Research Involving Human Subjects: Overview of International Guidelines Maria Fidelis C. Manalo, MD, MSc Epidemiology
222 views
Use of a Short Form For inclusion of non-English speaking participants in human subject research * To play the presentation, click on the icon on the
215 views
Using the short form and reporting adverse events Erin Coons, Senior IRB Specialist, COMIRB 1
216 views
Institutional Review Board (IRB) Human Subject Dr. John N. Austin, Director and Ms. Renee S. Jones, Associate Director Delaware State University Office
216 views
Institutional Review Board (IRB) Human Subject Delaware State University Office of Sponsored Programs
219 views
Next >