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The top documents tagged [effective informed consent]

Youve been WARNED…. Everyday occurrences that landed your colleagues with a Warning Letter from the FDA Laura B. Cummins, J.D. Manager, Contract Administration
Youve been WARNED…. Everyday occurrences that landed your colleagues with a Warning Letter from the FDA Laura B. Cummins, J.D. Manager, Contract Administration
218 views
Informed Consent Ethics Forum 2012 Duquesne University Thomas Goehring, Leah Gottlieb, Andrew Glaid, Sebastien Hebert, David George Mentor: Dr. Mike Cascio
Informed Consent Ethics Forum 2012 Duquesne University Thomas Goehring, Leah Gottlieb, Andrew Glaid, Sebastien Hebert, David George Mentor: Dr. Mike Cascio
222 views
COMMON PROBLEMS IN INFORMED CONSENT Jeri R. Barney, JD, MS Michele Antisdel, MBA/CCRP HRPP Compliance ManagerIRB Regulatory Analyst Human Research Protection
COMMON PROBLEMS IN INFORMED CONSENT Jeri R. Barney, JD, MS Michele Antisdel, MBA/CCRP HRPP Compliance ManagerIRB Regulatory Analyst Human Research Protection
247 views
DF/ HCC DANA-FARBER / HARVARD CANCER CENTER Beth Israel Deaconess Medical Center / Brigham and Women’s Hospital / Children’s Hospital Boston / Dana-Farber
DF/ HCC DANA-FARBER / HARVARD CANCER CENTER Beth Israel Deaconess Medical Center / Brigham and Women’s Hospital / Children’s Hospital Boston / Dana-Farber
216 views
FDA Warning Letters - Slide 1
FDA Warning Letters - Slide 1
1.478 views
INFORMED CONSENT: PROCESS, DOCUMENTATION, ALTERATION AND WAIVERS Suzanne Sparrow
INFORMED CONSENT: PROCESS, DOCUMENTATION, ALTERATION AND WAIVERS Suzanne Sparrow
217 views
SACHRP Strauss Flynn 7-08 Subcommittee on the Inclusion of Individuals with Impaired Decision- making in Research [SIIIDR] Presentation to SACHRP July
SACHRP Strauss Flynn 7-08 Subcommittee on the Inclusion of Individuals with Impaired Decision- making in Research [SIIIDR] Presentation to SACHRP July
213 views
Identify consent process requirements Distinguish between IRB, PI/Designee consent process responsibilities Identify with what went wrong? Summarize
Identify consent process requirements Distinguish between IRB, PI/Designee consent process responsibilities Identify with what went wrong? Summarize
220 views
Clinical Research and Regulations Marilyn Marshall QAO Office of the Vice President of Research
Clinical Research and Regulations Marilyn Marshall QAO Office of the Vice President of Research
219 views
Columbia University Medical Center Research Billing Compliance presented by Office for Billing Compliance Research Billing Compliance presented by Office
Columbia University Medical Center Research Billing Compliance presented by Office for Billing Compliance Research Billing Compliance presented by Office
225 views
Part 1 of 3 Part Series: Informed Consent: The Document Wendy Lloyd, BA, LPN, CIP, CCRP Regulatory Affairs and Compliance Specialist Process Improvement
Part 1 of 3 Part Series: Informed Consent: The Document Wendy Lloyd, BA, LPN, CIP, CCRP Regulatory Affairs and Compliance Specialist Process Improvement
223 views
Recommendations from the Subcommittee on the Inclusion of Individuals With Impaired Decision-making in Research (SIIIDR) March 27, 2008 David H Strauss,
Recommendations from the Subcommittee on the Inclusion of Individuals With Impaired Decision-making in Research (SIIIDR) March 27, 2008 David H Strauss,
226 views