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Course Description

This course provides an introduction to good clinical practice (GCP) in clinical research according to FDA regulations and International Conference on Harmonization (ICH) guidelines. Topics include conducting clinical trials in accordance with GCP; regulations established by state, federal, and international regulatory bodies; and the roles and responsibilities of investigators, sponsors, monitors, and auditors.

Online self-paced: Refers to course start and end dates.

Online fixed date: Refers to synchronous session schedule fully available under “Section Notes”.

Prerequisites

none

Applies Toward the Following Certificates

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Enroll Now - Select a section to enroll in
Section Title
Good Clinical Practices
Type
Online, self-paced
Dates
Jun 10, 2024 to Jul 10, 2024
Contact Hours
7.5
Location
  • Online
Delivery Options
Course Fee(s)
Tuition Fees non-credit $1,435.00
Section Notes

Synchronous sessions are conducted on Wednesdays from 6:00 to 7:30 p.m. CST.

Specific dates: June 12, 18, 26, July 3, and 10.

Section Title
Good Clinical Practices
Type
Online, self-paced
Dates
Aug 12, 2024 to Sep 11, 2024
Contact Hours
7.5
Location
  • Online
Delivery Options
Course Fee(s)
Tuition Fees non-credit $1,435.00
Section Notes

Synchronous sessions are conducted on Wednesdays from 6:00 to 7:30 p.m. CST.
Specific dates: August 14, 21, 28, September 4, and 11.

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