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The top documents tagged [good clinical practices]

Multi-regional Clinical Trials Why be concerned ? A Regulatory Perspective on Issues Robert T. O’Neill Ph.D. Director, Office of Biostatistics Office of
Multi-regional Clinical Trials Why be concerned ? A Regulatory Perspective on Issues Robert T. O’Neill Ph.D. Director, Office of Biostatistics Office of
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“Good Clinical Practices” in Meeting Regulatory Responsibilities Terry VandenBosch, RN, PhD, CIP, CCRP Senior Research Compliance Associate Office of Human
“Good Clinical Practices” in Meeting Regulatory Responsibilities Terry VandenBosch, RN, PhD, CIP, CCRP Senior Research Compliance Associate Office of Human
218 views
Ethical Issues in Translational Research Emma A. Meagher, MD emma@gcrc.upenn.edu
Ethical Issues in Translational Research Emma A. Meagher, MD [email protected]
216 views
General Principles for Meeting Regulatory Responsibilities Terry VandenBosch, RN, PhD, CIP, CCRP Senior Research Compliance Associate Office of Human Research
General Principles for Meeting Regulatory Responsibilities Terry VandenBosch, RN, PhD, CIP, CCRP Senior Research Compliance Associate Office of Human Research
217 views
Prevention of HIV in Health Care Facilities Dr KANUPRIYA CHATURVEDI
Prevention of HIV in Health Care Facilities Dr KANUPRIYA CHATURVEDI
222 views
© LTB, June 2006 Nationwide CCOPD Initiative Clinical Trial Management System Yvan Fortier Biomedical Telematics Laboratory of the RHN (LTB) with the collaboration
© LTB, June 2006 Nationwide CCOPD Initiative Clinical Trial Management System Yvan Fortier Biomedical Telematics Laboratory of the RHN (LTB) with the collaboration
216 views
Good Clinical Practices and FDA Inspections Patricia Holobaugh Chief, Bioresearch Monitoring Branch Division of Inspections and Surveillance Office of
Good Clinical Practices and FDA Inspections Patricia Holobaugh Chief, Bioresearch Monitoring Branch Division of Inspections and Surveillance Office of
228 views
Research ethics HRH Research Forum Dr Muna I Abdel Aziz MBBS, MD, MPH, PhD, CCST, FFPH Session developed 10 March 2012
Research ethics HRH Research Forum Dr Muna I Abdel Aziz MBBS, MD, MPH, PhD, CCST, FFPH Session developed 10 March 2012
218 views
Monitoring and Special Considerations for Multi-Center Trials September 10, 2010 Pav Aujla, MS, CCRP, RAC Primo N. Lara, Jr. MD A Translational Innovation
Monitoring and Special Considerations for Multi-Center Trials September 10, 2010 Pav Aujla, MS, CCRP, RAC Primo N. Lara, Jr. MD A Translational Innovation
216 views
Dealing with the FDA – The Pharma Experience Uwe P. Trinks, Ph.D TMA Annual Meeting, Williamsburg, VA
Dealing with the FDA – The Pharma Experience Uwe P. Trinks, Ph.D TMA Annual Meeting, Williamsburg, VA
214 views
FDLI February 11, 2008 Bradley Merrill Thompson Managing and Complying with Clinical Trial Quality Obligations for Sponsors
FDLI February 11, 2008 Bradley Merrill Thompson Managing and Complying with Clinical Trial Quality Obligations for Sponsors
217 views
Scientific Data for Evidence- Based Drug Regulation Janet Woodcock, M.D. Director, Center for Drug Evaluation and Research Food and Drug Administration
Scientific Data for Evidence- Based Drug Regulation Janet Woodcock, M.D. Director, Center for Drug Evaluation and Research Food and Drug Administration
220 views