Monitoring Clinical Trials for GCP Compliance
Agenda: Day One
I. Explore Clinical Trial Design
II. Defining "Good Clinical Practice" (GCP)
III. Writing & Using Standard Operating Procedures (SOPs) in Clinical Trials
IV. Protection of Human Subjects in Clinical Trials
V. The Investigator's Role in a Clinical Trial
VI. Understand The Role of the Institutional Review Board (IRB)
Booking Options
This course is available exclusively as an onsite training solution. To discuss a solution that fits your organization's needs, objectives, schedule and budget, contact a PTi Client Solutions Manager at 800-303-8194 or OnSiteSolutions@pti-international.com.