'Clinical investigators' diaporamas de présentation

Good Clinical Practice and Audit Preparedness

Good Clinical Practice and Audit Preparedness. IUPU Symposium - October 2010. Michael R. Hamrell, Ph.D. MORIAH Consultants. What is Clinical Research?. The essential piece to demonstrate that a new product is safe and effective The most costly part of development

1.19k views • 83 slides

Clinical Research in the Emergency Department

Clinical Research in the Emergency Department. Jim Quinn MD MS Associate Professor of Surgery/Emergency Medicine Research Director Emergency Medicine. Overview. Goals for research in academic emergency medicine Problems/solutions for researchers in emergency medicine

780 views • 54 slides

Taking GCP Training to a New Level:

Taking GCP Training to a New Level:. Making a Bottom Line Impact Ruth Ann Nylen, PhD The RAN Institute Paul Mastoridis, Pharm D Schering-Plough Corporation. Ruth Ann Nylen, PhD The RAN Institute Tampa, FL. Discussion Topics.

912 views • 51 slides

How Young Faculty Can Avoid Common Pitfalls in Academic Life

How Young Faculty Can Avoid Common Pitfalls in Academic Life. David Robertson, MD CRC Director March 16, 2007. Limited Focus of this Presentation. Medical School Clinical Department Physician Investigators Role of the physician Role of the investigator. Outline. Clinical Research

1.18k views • 49 slides

Recent Developments in FDA Regulation of Clinical Trials: ClinicalTrials.gov and Future FDA Proposals

Recent Developments in FDA Regulation of Clinical Trials: ClinicalTrials.gov and Future FDA Proposals. International Pharmaceutical Regulatory and Compliance Congress and Best Practices Forum. Linda R. Horton, Partner Hogan & Hartson, LLP Washington, DC/Brussels May 28, 2008.

949 views • 45 slides

Negotiating the Family Justice Maze: A Cooperative Approach

588 views • 41 slides

Application of Genetic Tools to Clinical and Translational Research

Application of Genetic Tools to Clinical and Translational Research. Thomas A. Pearson, MD, PhD University of Rochester School of Medicine Visiting Scientist, NHGRI. TAProots Vineyard Keuka Lake, NY. Concord Grapes. One year old French hybrid grapes. Vanessa Seedless Grapes.

625 views • 39 slides

Johns Hopkins Institute for Clinical and Translational Research A CTSA Program

Johns Hopkins Institute for Clinical and Translational Research A CTSA Program. Daniel E. Ford, M.D., M.P.H. Director, Institute for Clinical and Translational Research Vice Dean for Clinical Investigation. Goals for the Presentation. Introduce national and local CTSA program

604 views • 38 slides

Mapping Your Career With NIH Henry Khachaturian, Ph.D. Extramural Program Policy Officer Office of Extramural Research,

NIH Office of Extramural Research. Mapping Your Career With NIH Henry Khachaturian, Ph.D. Extramural Program Policy Officer Office of Extramural Research, NIH Email: hk11b@nih.gov. National Institutes of Health.

589 views • 36 slides

UKCRC Registered Clinical Trials Unit Network

UKCRC Registered Clinical Trials Unit Network. UKCRC CTU Registration. CTU Workshop, January 2012. Presented by Professor Julia Brown UKCRC Registered CTU Network . Unprecedented investment in clinical research in recent years - expansion in UK clinical trials portfolio

483 views • 29 slides

Psychoactive Botanical Products: A Workshop Sponsored by NIDA and ODS

Psychoactive Botanical Products: A Workshop Sponsored by NIDA and ODS Paul M. Coates, Ph.D. Director, Office of Dietary Supplements National Institutes of Health Department of Health and Human Services DSHEA (Dietary Supplement Health and Education Act - 1994) Amended the FD & C Act

500 views • 24 slides

Virtual/Accelerated Drug Development A better approach to product development!

Virtual/Accelerated Drug Development A better approach to product development!. Robert G. Burford, Ph.D. Managing Director Aptuit Consulting Inc. Drug development is a REGULATED RESEARCH activity!!. Creation of drug substance Preclinical characterization of drug substance .

412 views • 24 slides

Intramural Research Program Administrative Review Followup Barry Hoffer, M.D., Ph.D. Director, Division of Intramural Re

Intramural Research Program Administrative Review Followup Barry Hoffer, M.D., Ph.D. Director, Division of Intramural Research, NIDA February 4, 2009. Administrative Review.

405 views • 21 slides

Informed Consent: Process, Documentation, Alteration and Waivers

Informed Consent: Process, Documentation, Alteration and Waivers. Suzanne Sparrow. Objectives. Significance & History Regulations (DHHS/FDA) Elements of Consent Waiving/altering consent Waiving documentation of consent Process of consent

325 views • 18 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

288 views • 17 slides

Intramural Clinical Research Steering Committee (ICRSC): Presentation to the National Cancer Advisory Board February 3,

Intramural Clinical Research Steering Committee (ICRSC): Presentation to the National Cancer Advisory Board February 3, 2009. Daniel Kastner, MD, PhD NIH Deputy Director for Intramural Clinical Research. The Issues: Optimizing Clinical and Translational Research in the IRP.

464 views • 15 slides

Aims & Scope

Aims & Scope Clinical Investigation is dedicated to systematic coverage of the methodology, progress and outcomes of clinical trials.

274 views • 15 slides

The Informed Consent Zone

The Informed Consent Zone. Patricia S. Kerby, MPA Office of Research Compliance September 10, 2008. Principles of Informed Consent. Researchers must make sure patients understand the difference between clinical research and standard therapy. Principles cont.

327 views • 12 slides

Masters in Clinical Research

258 views • 10 slides

201 views • 6 slides