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The top documents tagged [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.,
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
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
214 views
ICH Harmonised Tripartite Guideline for Good Clinical Practice Part I (Principles, IRB/IEC, Investigator, Sponsor) Josip Arlica, MD Altiora Training Program
ICH Harmonised Tripartite Guideline for Good Clinical Practice Part I (Principles, IRB/IEC, Investigator, Sponsor) Josip Arlica, MD Altiora Training Program
231 views
Au Psy492 E Portfolio Template For Slide Share
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
Ten Fatal Flaws of NIH Grant Submissions (and how to avoid them) Steffanie A. Strathdee, PhD Thomas L. Patterson, PhD
217 views
Institutional Review Board Guidance. Independent Ethics Committee Ethical Review Board Research Ethics Committee 2
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
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)
Advanced Topics in the Submission of Research Protocols to the Institutional Review Board (IRB) and the Office for the Protection of Human Subjects (OPHS)
216 views
KFDA Inspection Program for Quality and Compliance Efforts Young-Ok Kim Clinical Trials Management Div. Korea Food and Drug Administration
KFDA Inspection Program for Quality and Compliance Efforts Young-Ok Kim Clinical Trials Management Div. Korea Food and Drug Administration
218 views
Human Subjects Protection Committee at Cal Poly Pomona The Institutional Review Board Bruce W. Kennedy, MS RLATG CMAR Compliance Associate IRB Administrator
Human Subjects Protection Committee at Cal Poly Pomona The Institutional Review Board Bruce W. Kennedy, MS RLATG CMAR Compliance Associate IRB Administrator
218 views
Quality Improvement & Research
Quality Improvement & Research
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University of Toledo Department for Human Research Protection and Institutional Review Boards
University of Toledo Department for Human Research Protection and Institutional Review Boards
216 views