Training

BASIC RESEARCH TRAINING

Research History and Background, Evolution of Regulations and Guidance

Janie Gardner, MS, CCRP, CIM

Phases of Clinical Research and Study Types

Janie Gardner, MS, CCRP, CIM

Good Clinical Practice, ICH Guidelines, Compliance, FDA Regulations

Derita Bran, MSN, RN, CCRC

Standard Operating Procedures

Marie Jackson, PhD, MBA

Role and Responsibilities of the IRB, Sponsor, CRO, Principal Investigators, and Key Study Personnel

Derita Bran, MSN, RN, CCRC

Download Powerpoint or Watch Presentation

Informed Consent / Assent and Documentation of the Informed Consent Process

Margaret Lynn, LMSW, RDN, CCRP, CIP

Watch Video