'Ind ide' presentation slideshows

Good Clinical Practice: Are We There Yet ? And What Comes Next ?

Good Clinical Practice: Are We There Yet ? And What Comes Next ?. David A. Lepay, MD PhD Senior Advisor for Clinical Science Office of the Commissioner, US FDA July 25, 2007. What This Talk Will Cover. Introduction to FDA FDA Expectations and Oversight in Clinical Research

634 views • 41 slides

IRB Minutes & Records VA Requirements

IRB Minutes & Records VA Requirements. Kevin L. Nellis, M.S., M.T. (A.S.C.P.) Program Analyst Program for Research Integrity Development and Education (PRIDE). VHA Handbook 1200.05 Sets the Floor, not the Ceiling. Follow state and local laws when more stringent

503 views • 38 slides

IRB Minutes & Records VA Requirements

IRB Minutes & Records VA Requirements. Kevin L. Nellis, M.S., M.T. (A.S.C.P.) Program Analyst Program for Research Integrity Development and Education (PRIDE). VHA Handbook 1200.05 Sets the Floor, not the Ceiling. Follow state and local laws when more stringent

472 views • 38 slides

HRPP Policies & Forms Chapter Two

HRPP Policies & Forms Chapter Two. Created/Revised for AAHRPP June 1, 2007. REVISED POLICIES. Revised Policy. SOP 202 Management of IRB The performance of the IRB Chairs, Vice Chairs, and IRB Members shall be evaluated on an annual basis.

603 views • 36 slides

Exception to Informed Consent Under Emergency Circumstances (21 CFR 50.24)

Exception to Informed Consent Under Emergency Circumstances (21 CFR 50.24). Tom P. Aufderheide, M.D., FACEP, FAHA Professor of Emergency Medicine Associate Chair of Research Affairs Medical College of Wisconsin. Presenter Disclosure Information. Tom P. Aufderheide, M.D., FACEP, FAHA

490 views • 17 slides

Current structure of review of Human Research Protocols that involve ionizing radiation

194 views • 9 slides