CME Sponsor:
Pharmaceutical Education and Research Institute (PERI) 

Location:
It is a web-based CME activity

Course Directors/Instructors:
Phyllis J. Panico, PhD
Retired Manager of Professional Development
AstraZeneca, LP

Cheryl J. Priest, RN,
Independant Clinical Development Training
and Quality Process Consultant

Number of Credits:

ACPE: 1.5 CEU
VNA: 04-04-05 14.40 Contact Hours

Registration Fee:
Regular Registration Fee: $590
ACS/Gov Registration Fee: $490
Cancellation Fee: $100

More Info

Detailed Description:

The goal of this course is to provide a practical orientation to site management and monitoring of clinical studies. The course provides a comprehensive overview of clinical monitoring in the context of the overall drug development process; FDA and HPB regulations; and ICH guidelines for GCP. This course will be delivered completely over the Internet, which means you will progress at your own pace through the course content.

The course combines text-based study materials with interactive exercises enabling you to apply what you have learned to on-the-job situations. You should expect to spend approximately 15 hours of study time to complete the course. You will have a four-month access after you register for the course.