Writing SOPs for Clinical Research
Agenda: Day One
I. Review Essential GCP Requirements
II. Analyze Current FDA Regulatory Actions for Compliance with GCP Standards
III. Determine Why Writing is an Art and Not a Science
IV. Evaluate Policies: Interpreting Regulations to Guide Operations
V. Describe the SOP Construction and Organization Process
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.