×
Log in
Upload File
Most Popular
Art & Photos
Automotive
Business
Career
Design
Education
Hi-Tech
+ Browse for More
The top documents tagged [report adverse events]
Documents
FDA Compliance Actions Against IRBs and Clinical Investigators Paul W. Goebel, Jr., CIP Vice President
[email protected]
Chesapeake Research Review,
220 views
Documents
Office of Research Oversight 1 VHA Handbook 1058.01 Research Compliance Reporting Requirements Revised May 21, 2010 (Presentation prepared for HRPP 101,
230 views
Documents
Overview of Good Clinical Practice (GCP) Investigator Responsibilities
50 views
Documents
University of Miami Office of Research Compliance Assessment Lynn E. Smith, JD, CIM, CIP Johanna Stamates, RN, BA, CCRC With assistance from Elizabeth
215 views