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The top documents tagged [fda center]

What are the FDA Regulatory Requirements for Importing Medical Devices into the U.S.? Carole C. Carey carole.carey@fda.hhs.gov Director, CDRH International
What are the FDA Regulatory Requirements for Importing Medical Devices into the U.S.? Carole C. Carey [email protected] Director, CDRH International
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1 FDA’s BIMO Inspection Program and IRB Inspections VA IRB Chairs Meeting August 2012 Janet Donnelly RAC, CIP Office of Good Clinical Practice Office of
1 FDA’s BIMO Inspection Program and IRB Inspections VA IRB Chairs Meeting August 2012 Janet Donnelly RAC, CIP Office of Good Clinical Practice Office of
220 views
2009 08 15 Vaccines, Adverse Reactions, and the Florida Law
2009 08 15 Vaccines, Adverse Reactions, and the Florida Law
1.759 views
Some Important Drugs for Cholesterol and Hypertension
Some Important Drugs for Cholesterol and Hypertension
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1 Tobacco Constituents: Discussion of Abuse Liability Allison C. Hoffman, Ph.D. FDA Center for Tobacco Products July 7-8, 2010
1 Tobacco Constituents: Discussion of Abuse Liability Allison C. Hoffman, Ph.D. FDA Center for Tobacco Products July 7-8, 2010
216 views
Overview of Drug Development: the Regulatory Process Roger D. Nolan, PhD Director, Project Operations Calvert Research Institute November, 2006 Roger D
Overview of Drug Development: the Regulatory Process Roger D. Nolan, PhD Director, Project Operations Calvert Research Institute November, 2006 Roger D
215 views
UCSD SAN DIEGO SUPERCOMPUTER CENTER TeacherTECH Summer Science July 1, 2005 Dr. Joseph M. Cleary Project Manager, San Diego Supercomputer Center, UCSD
UCSD SAN DIEGO SUPERCOMPUTER CENTER TeacherTECH Summer Science July 1, 2005 Dr. Joseph M. Cleary Project Manager, San Diego Supercomputer Center, UCSD
216 views
Toxicology in Drug Development Lynnda Reid, Ph.D. Pharmacology/Toxicology Reviewer Center for Drug Evaluation and Research (CDER) Rafael Ponce, Ph.D.,
Toxicology in Drug Development Lynnda Reid, Ph.D. Pharmacology/Toxicology Reviewer Center for Drug Evaluation and Research (CDER) Rafael Ponce, Ph.D.,
233 views
MAGI's Clinical Trial Agreements, Budgets & Regulatory Conference FDA Inspections of Investigator Sites Paul Below Clinical Research Consultant P. Below
MAGI's Clinical Trial Agreements, Budgets & Regulatory Conference FDA Inspections of Investigator Sites Paul Below Clinical Research Consultant P. Below
258 views
CHOOSING A PET FOOD By C Kohn - Agricultural Sciences, Waterford WI Based on Interpreting Pet Food Labels, by Dr. Dzanis, DVM, USDAInterpreting Pet Food
CHOOSING A PET FOOD By C Kohn - Agricultural Sciences, Waterford WI Based on Interpreting Pet Food Labels, by Dr. Dzanis, DVM, USDAInterpreting Pet Food
234 views
Biomedical Device Security: New Challenges and Opportunities Florence D. Hudson Senior Vice President and Chief Innovation Officer Internet2 June 22, 2015
Biomedical Device Security: New Challenges and Opportunities Florence D. Hudson Senior Vice President and Chief Innovation Officer Internet2 June 22, 2015
214 views
Regulatory Issues. Introduction to the Regulatory Approval Process; Overview of the FDA Investigational New Drug Application (IND); Summary of regulations
Regulatory Issues. Introduction to the Regulatory Approval Process; Overview of the FDA Investigational New Drug Application (IND); Summary of regulations
226 views