'Data safety monitoring board' presentation slideshows

Welcome! Donor Management Research Consensus Conference

Welcome! Donor Management Research Consensus Conference. September 16-17, 2013 Arlington, VA. Note: This document is not intended as final recommendation. . Conference Co-Chairs. Peter L. Abt, MD

887 views • 77 slides

Clinical Trials at USC Protecting Human Research Subjects

Clinical Trials at USC Protecting Human Research Subjects. Susan L. Rose Executive Director Office for the Protection of Research Subjects. Join RC Network. Lunch and Learn with USC VIPs Focus: EMR , Monitor Access, Part 11 and CTO Date: 3/14/14 at 12pm | Norris Topping Tower 7409

591 views • 39 slides

1.06k views • 37 slides

New Adverse Event Reporting Policy

New Adverse Event Reporting Policy. Effective September 1, 2007. Local adverse event reporting. Local adverse events are those experienced by subjects enrolled by the investigator(s) at this institution or in the local community area

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Issues re: Adverse Events

467 views • 33 slides

Conflicts of interests for Leif Thuesen, M.D. Edwards Lifesciences: Physician proctor

A Prospective, Randomized Trial of Transapical Transcatheter Aortic Valve Implantation vs. Surgical Aortic Valve Replacement in Operable Elderly Patients with Aortic Stenosis The STACCATO Trial.

740 views • 27 slides

Disclosures

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Judd E. Hollander, MD Professor Clinical Research Director

One Year Outcomes and Resource Utilization in ACRIN PA 4005: Multicenter RCT of Rapid Rule-Out Strategy of CCTA vs Traditional Care . Judd E. Hollander, MD Professor Clinical Research Director . Funding & Disclosures. Funding

371 views • 25 slides

Study Monitoring: What Does It Mean & How To Do It Right

Study Monitoring: What Does It Mean & How To Do It Right. Partners Human Research Quality Improvement Program QUICK BITE Series December 9, 2004. Regardless Of Funding . . . They All Agree.

407 views • 24 slides

CLINICAL TRIALS IN NEW DRUG DEVELOPMENT

468 views • 23 slides

Design and Analysis of Clinical Study 12. Randomized Clinical Trials

Design and Analysis of Clinical Study 12. Randomized Clinical Trials. Dr. Tuan V. Nguyen Garvan Institute of Medical Research Sydney, Australia. Basic Design of Clinical Trials. Cured. Same. Treatment. Sample. Randomise. Blinding. Placebo. Cured. Same. Subjects. Blocking.

470 views • 20 slides

I.V. Enoxaparin or Unfractionated Heparin in Primary PCI: Acute and Long-term results

G. Montalescot, M. Cohen, P. Goldstein, K. Huber, C. Pollack, U. Zeymer , E. Vicaut for the ATOLL investigators. I.V. Enoxaparin or Unfractionated Heparin in Primary PCI: Acute and Long-term results.

453 views • 20 slides

FDA Public Hearing on Reporting of Adverse Events to Institutional Review Boards (21 March 2005)

FDA Public Hearing on Reporting of Adverse Events to Institutional Review Boards (21 March 2005). Presentation of Maureen Donahue Hardwick, Esquire on behalf of the IRB-Sponsor Roundtable. Introduction. Pleased to speak today on behalf of the IRB-Sponsor Roundtable

285 views • 19 slides

MOABO201. XIX International AIDS Conference 2012

Lipid profile in children randomized to immediate versus deferred nevirapine -based antiretroviral therapy in the PREDICT study. Kanjanavanit S , Puthanakit T , Kosalaraksa P, Hansudewechakul R , Ngampiyaskul C , Pinyakorn S , Luesomboon W, Saphonn V , Ananworanich J, Ruxrungtham K

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Decoding RFAs, RFPs, and PAs Charlotte Flipp Division of Epidemiology Anne Everett Division of Epidemiology

Decoding RFAs, RFPs, and PAs Charlotte Flipp Division of Epidemiology Anne Everett Division of Epidemiology Kevin McKoskey Sponsored Projects Administration. Topics for Discussion. PA (Program Announcement) RFA (Request for Application) RFP (Request for Proposal).

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Prof. Scott Emerson

179 views • 8 slides

The MADIT II Trial

The MADIT II Trial. Multicenter Autonomic Defibrillator Implantation Trial II Presented at the American College of Cardiology 51st Annual Scientific Session Atlanta, GA Arthur J. Moss, M.D. for the MADIT II investigators.

697 views • 6 slides