Clinical Trials.gov, How does it Affect Me? What Do I Need to Know?
Please click here to purchase your contact hour.
Speaker Name:Brian Phillips, Regulatory Systems Analyst
Target Audience
- CRCs
- Investigators
- Project Managers
- Regulatory Affairs/Compliance
- Quality Assurance
- Clinical Research Administrators
Program DescriptionWest Virginia Clinical and Translational Science Institute (WVCTSI) Center of Excellence Regulatory Systems Analyst, Mr. Brian Phillips will be providing an overview of ClinicalTrials.gov registration and reporting for investigators and their research teams. The reasons registration of trials is necessary will be discussed in detail in order to ensure compliance with all applicable regulations.
Program Agenda11:30 am –12:00 –Networking Opportunity-Lunch Provided
12:00 – 1:00 pm – Educational Presentation
Learning Objectives
- Demonstrate high level knowledge of the regulations and guidelines that require registration and results reporting of applicable clinical trials
- Describe why clinical trial registration reporting is beneficial
- Understand the high level process of obtaining an account on ClinicalTrials.gov and registering a trial.
- Understand the basics of reporting results
- Describe the penalties associated with non-compliance
Contact hours: 1.0 Contact hours have been applied for through ACRP.
Membership is not required for online registration of contact hours.
To receive contact hours: Purchase the contact hours, sign in at the event, and attend the program. Log on to the ACRP website then “My Courses” to complete the evaluation no later than 30 days following the event and obtain the online certificate.
Registration Cost: FREE to all Chapter Members, ACRP Members, Non-Members
Contact Hour Cost:
- $0 Chapter Members
- $15 ACRP Members
- $30 Non-Members
Refund Policy: Not applicable