Investigator Responsibilities in Clinical Research Melissa Adde Director, Clinical Trials Office, INCTR .
Responsible Conduct of Research, Scholarship, and Creative Activities Protection of Human Subjects Responsible Conduct of Research, Scholarship, and Creative.
The Importance of Standard Operating Procedures (SOPs) in ...
Top Ten Investigator Responsibilities When Conducting Human Subjects Research Thanks to Ada Sue Selwitz, Univ. of Kentucky and PRIM&R (Public Responsibility.
IRB’s Top Ten* Investigator Responsibilities What Every Investigator (and his/her research staff) (and his/her research staff) Should Know about Should.
1 Pharmacovigilance Lindsey Connery Pharmacovigilance Manager, Cancer Research UK Clinical Trials Unit, Glasgow.
1 Book Cover Here Copyright © 2014, Elsevier Inc. All Rights Reserved Criminal Investigation: A Method for Reconstructing the Past, 7 th Edition Criminal.
“Good Clinical Practices” in Meeting Regulatory Responsibilities Terry VandenBosch, RN, PhD, CIP, CCRP Senior Research Compliance Associate Office of Human.
1 Module 4. 2 History of Good Clinical Practice Regulations Barbara Novak.
Valid Informed Consent Education Pilot Project 2 nd Annual Nursing Research & Evidence-Based Practice Symposium Sandra Knowlton-Soho, MS, RN Sara Simeone,
HRPP Training – Session Two Michelle Brignac, CIP Human Research Protection Program Manager.
Clinical Research Responsibilities for NIDCR-Funded Investigators
