Course Description
This web seminar provides the basic concept of Good Clinical Practice (GCP). Participants will learn the goals of GCP and its common elements (FDA regulations and the ICH GCP E6 Guideline, including R3 updates) defining the quality system of mutual accountability between the sponsor, investigator, IRB/IEC, and the regulatory authority. The basic roles and responsibilities of each stakeholder will be discussed in relation to these criteria. The new principles of the ICH GCP E6 R3 Guideline will be discussed in a practical manner to ensure compliance with all regulatory requirements.
Learning Objectives
Who Should Attend
Instructor
The course will be led by one of the following instructors:
Lily Romero, P.A., C.C.R.C.
Elizabeth Weeks-Rowe, LVN, C.C.R.A.
Click here for complete trainer biographies
Registration Fees
$735*
*Includes up to 20 participants per login at a single location. All participants (up to 20) are eligible for “Certificates of Attendance,” and accreditation, provided that accreditation requirements are met. For groups larger than 20 or for additional logins for other locations, please call +1 781.972.5400 or toll-free in the U.S. 800.856.2556, or email customer.service@barnettinternational.com for pricing.
Accreditation Information
Barnett International is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education. Participants will receive 1.5 hours (0.15 CEUs) of continuing education credit for full participation, including the completion of a pre-test, post-test, and program evaluation. Barnett International will issue a receipt of completion for earned CEUs within three weeks of program completion. ACPE#: 0778-0000-23-048-L99-P. Released: 9/23.
Hold this course at your company! For more information, contact Naila Ganatra at +1 215.413.2471.