WebGood Clinical Practice: Training Resource: [Select any one of the following] Completion of on-line, interactive ACRP Good Clinical Practice (GCP) Simulation module; Completion of: CITI's GCP eLearning Module [CITI Drugs and Device and Social & Behavioral] Providing documentation of approved, sponsor-required GCP training WebNov 9, 2024 · training, good clinical practice, research human subject protection, informed consent, institutional review board, IRB, sponsor, trial, study, investigator
Clinical Research Coordinator - Orlando Health
WebThe principles of Good Clinical Practice (GCP) help assure the safety, integrity, and quality of clinical trials by addressing elements related to the design, conduct, and reporting of … WebGood Clinical Practice (GCP) training is required for all individuals involved in the conduct of clinical trials in any of the following categories: Biomedical clinical trials submitted for initial IRB approval on or after November 1, 2016, with any source of funding or support; and. Social-behavioral clinical trials that are submitted for ... iph 2015
CITI Program Training Research Protections Office The …
WebWhat are the goals of GCP? 1. To protect the rights, safety and welfare of humans participating in research. 2. To assure the quality, reliability and integrity of data collected. 3. To provide standards and guidelines for the conduct of clinical research. 4. Good Clinical Practice = Ethics + Quality Data. WebSep 25, 2015 · The CITI Good Clinical Practice (GCP) Optional Modules Course is a 13-module program that discusses good clinical practice as it relates to clinical trials of … WebSep 25, 2015 · The CITI Good Clinical Practice (GCP) Optional Modules Course is a 13-module program that discusses good clinical practice as it relates to clinical trials of both drugs/biologics as well as devices. The GCP modules are described below and are intended for use by research personnel involved in conducting drug, device, or biologic studies and ... iph 2018