ICH E6(R2) GCP Training for Investigator Site Personnel
ICH E6(R2) GCP Training for Investigator Site Personnel
To purchase access for your team, or if you have any questions, email us at info@clinicalpathwaysresearch.com.
Course outline HERE
INTERACTIVE DEMO AVAILABLE BELOW
This Investigator Site Personnel Good Clinical Practice (GCP) course covers the requirements of GCP for clinical trials found in ICH E6(R2) related to the role of the investigator and site personnel and briefly covers roles of other stakeholders.
This ICH E6 (R2) GCP Training meets the Minimum Criteria for ICH GCP Investigator Site Personnel Training identified by TransCelerate BioPharma as necessary to enable mutual recognition of GCP training among trial sponsors.
Course Length: 60 minutes
INCLUDES:
Unlimited access to the content for 45 days from your initial day of purchase.
Certificate of completion
Case Studies
Post-Assessment
Knowledge Checks
LEARNING OBJECTIVES
Discover the Global Good Clinical Practice Guideline ICH E6(R2) and how it affects your role.
Reflect on challenges and opportunities in implementing the GCP Guideline.
Identify practical applications of the Guideline in your work processes.
AUDIENCE
All investigator site personnel
INTERACTIVE DEMO:
