Complying with 21 CFR for Clinical Research
Agenda: Day One
I. Overview of 21 CFR Part 11
II. Clarify the Impact of 21 CFR Part 11 on Your Electronic SOPs
III. Ensure Optimal Data Collection
IV. Interpret 21 CFR Part 11 in Relation to Documentation Training Records, and Validation of Clinical Data
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.