Page Style:
Background Pattern:
Sub Menu:
Containers Header 1:
Containers Header 2:
Heading 1:
Heading 2:
Link - Mouse Over:
Cart Summary
Your shopping cart is empty.
Product Qty Amount

Monitor Role-Based Package

For: New monitors and those who need to review the fundamentals of clinical research regulations

Provide an understanding of clinical research procedures and requirements that is based in regulations. Help monitors prioritize tasks during site visits and help the trial progress while off site. Understand what FDA inspectors need to know and be able to provide them with information as requested. Gain the confidence to answer questions or challenges regarding research procedures.

The approximate time to complete each course and quiz is noted next to each course topic.

Upon successful completion of this course package, learners will receive 10.5 continuing education contact hours.


a.    Monitoring Overview - (40 minutes)

b.    Foundation Package                            
    i.    An Introduction to the U.S. FDA Regulations
        1.     Part I: 21 CFR Part 312 and 812 - (55 minutes)
        2.     Part II: 21 CFR Parts 50, 56, 54, and 11 - (40 minutes)
        3.     Comparing 21 CFR Parts 312 and 812 - (55 minutes)
    ii.    Good Clinical Practice
        1.     The History of Clinical Research - (60 minutes)
        2.     Introduction to Good Clinical Practice - (40 minutes)
        3.     The FAIR Shake(TM) Method  - (35 minutes)
    iii.    Human Subjects Protection
        1.     Human Subjects Protection: Drilling Down 21 CFR Part 50 - (40 minutes)
        2.     Introduction to HIPAA/HITECH - (40 minutes)

c.    Monitoring 101 Package
    i.    Site Assessment Visits - (55 minutes)
    ii.   Site Initiation Visits - (45 minutes)
    iii.  Periodic Monitoring Visits - (45 minutes)
    iv.  Close-Out Visits - (30 minutes)
    v.   Site Management - (30 minutes)

d.    Monitoring 102 Package
    i.     How to Review Informed Consent - (35 minutes)    
    ii.    How to Review Essential Documents - (40 minutes)
    iii.   How to Verify Source Data - (45 minutes)
    iv.   How to Conduct Product Accountability - (40 minutes)
    v.    Risk-Based Monitoring Overview - (45 minutes)