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The top documents tagged [safety of subjects]
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safety of subjects
20070327 1/50CERTIFICATION OF INVESTIGATORS JHGJ/gh CERTIFICATION OF (CLINICAL) INVESTIGATORS Prof. JanHasker G. Jonkman, Ph.D., F.C.P., F.R.Q.A., R.Ph.,
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1November 18, 20141 Collecting and Protecting Sensitive Data in Research CU Morningside IRB Joyce Plaza MS, MBE, CIP 419 West 119 Street New York, NY 10027.
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ICH Harmonised Tripartite Guideline for Good Clinical Practice Part I (Principles, IRB/IEC, Investigator, Sponsor) Josip Arlica, MD Altiora Training Program.
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Au Psy492 E Portfolio Template For Slide Share
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Ten Fatal Flaws of NIH Grant Submissions (and how to avoid them) Steffanie A. Strathdee, PhD Thomas L. Patterson, PhD.
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Institutional Review Board Guidance. Independent Ethics Committee Ethical Review Board Research Ethics Committee 2.
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1 Module 4. 2 History of Good Clinical Practice Regulations Barbara Novak.
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Advanced Topics in the Submission of Research Protocols to the Institutional Review Board (IRB) and the Office for the Protection of Human Subjects (OPHS)
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KFDA Inspection Program for Quality and Compliance Efforts Young-Ok Kim Clinical Trials Management Div. Korea Food and Drug Administration.
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Human Subjects Protection Committee at Cal Poly Pomona The Institutional Review Board Bruce W. Kennedy, MS RLATG CMAR Compliance Associate IRB Administrator.
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University of Toledo Department for Human Research Protection and Institutional Review Boards.
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Criteria For Approval 45 CFR 46.111 21 CFR 56.111 Minimized risks Reasonable risk/benefit ratio Equitable subject selection Informed consent process Informed.
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