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The top documents tagged [informed consent requirements]
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informed consent requirements
Vasopressin CPR Trial Community Consultation
289 views
Ethical Considerations Associated with Investigator Payments & Patient Recruitment Ginger Clasby - EVP, Business Development Promedica International Costa.
227 views
Compliance Considerations in Pharmaceutical Product Development Compliance Considerations in Pharmaceutical Product Development John C. (Jack) Garvey,
219 views
FDA Compliance Actions Against IRBs and Clinical Investigators Paul W. Goebel, Jr., CIP Vice President
[email protected]
Chesapeake Research Review,
217 views
Evaluating Minimal Risk: Time to Adopt a Uniform Standard Celia B. Fisher, Ph.D. Marie Ward Doty Professor of Psychology Director Center for Ethics Education.
213 views
Legislative Planning for 2008 Medical Society of the State of NY
209 views
Proposal to Modify Existing or Establish New Requirements for the Informed Consent of Living Donors (Resolution 18) Living Donor Committee Mary Amanda.
218 views
THE UNIVERSITY OF NEW MEXICO ▪ HEALTH SCIENCES CENTER Clinical and Translational Science Center (CTSC) 4/2009.
215 views
Institutional Review Board for Human Subject Research: Does Your Research Need One? Merle Rosenzweig
[email protected]
[email protected]
Michael Unsworth.
214 views
UCSF-CDDS 2007 Role of FDA in Guiding Drug Development Carl Peck Center for Drug Development Science UCSF, UC-Washington Center Washington DC Principles.
216 views
Radiological Devices Advisory Committee Meeting November 18, 2009 John A. DeLucia iCAD, Inc.
213 views
AMERICAN CONFERENCE INSTITUTE 12 th National Conference On Managing Legal Risks And Conducting Clinical Trials New York City February 24, 2010 Michael.
212 views