Clinical Protocol Development Series
The goal of this two day series is to provide researchers with knowledge, tools and resources to aid in the development of a scientific protocol for a clinical research study. Both sessions will begin at 9:00 AM and a question-and-answer session will follow each presentation.
On the second day of the series we will take a "deeper dive" into clinical study design, statistics, and their impact on clinicaltrials.gov reporting:
- Clinical Protocol Study Design
- aims, objectives, endpoints, and outcomes
- Statistical Analysis, sample size considerations, data management
- Clinicaltrials.gov
- outcome measure reporting
- Protocol problem spots and ways to improve protocols
ACRP Contact Hours: 4.0 Contact Hours of clinical research education on application for maintenance of ACRP's ccrc®, ccra® or cpi®, certification designations will be available for attendees
If you have any questions, please contact Marie Rape at This email address is being protected from spambots. You need JavaScript enabled to view it..