Conflict and Consent: Managing Disclosure in Human Subjects Research University of Miami Human Subjects Research Office Conflict of Interest Symposium.
Pharmacists Responsibilities in Clinical Studies Mike R Sather, PhD Crystal L Harris, PharmD February 26, 2004.
SCRIHS Training Presented by: Erin Campbell Alisha Mirabile Gary Fifer.
Introduction to the Institutional Review Board (IRB): Minnesota State University, Mankato Patricia M. Hargrove, Ph.D. IRB Coordinator Anne Blackhurst,
UC DAVIS OFFICE OF RESEARCH Overview of Good Clinical Practices (GCP) Investigator and Study Team Responsibilities Miles McFann IRB Administration Training.
1/33. What is INDA ? Types of INDAs Objectives of INDAs Format & Contents of an INDA IND Safety reports IND Annual Reports IND Review Process.
Bioterrorism: Changing Priorities in Medical Training and Research
Overview of Good Clinical Practice (GCP) Investigator Responsibilities
University of Miami Office of Research Compliance Assessment Lynn E. Smith, JD, CIM, CIP Johanna Stamates, RN, BA, CCRC With assistance from Elizabeth.
Protection of Human Subjects Case #2 Salim Darwiche Jean-Bernard Nobs Marco Pisano Anders Sandholm Valentina Triacca Responsible Conduct in Biomedical.
Preparing for an FDA Inspection Kathy Gilmartin, MSN, CRNP, CCRC Manager of Clinical Trials Quality Assurance.
INVESTIGATOR RESPONSIBILITIES March 2015. Objectives Review and Discuss: Responsibilities of the clinical research Investigator as per relevant regulations.
