Using e-Regulatory to Reduce Regulatory Burden
Speaker: Leslie Korbee
Registration Fees: Free and open to all to attend.
Program Agenda:
- 6:00 - 6:30pm- Registration & Networking
- 6:30 – 7:30 pm – Educational Presentation
- 7:30 - 8:00pm– Additional Discussion
Program Description: As an answer to many research sites drowning in regulatory paperwork as a result of clinical trials becoming increasingly more complex, eREG is on to consider. This intermediate-level course outlines the basics of eREG, document storage, and where and how to initiate implementation. The speaker will also list specific tools and resources that may be used to facilitate eREG.
Learning Objectives:
- Describe the background and an overview of eREG
- Define Electronic Document Storage: the Big Picture
- Identify the basics of getting started with eREG
- List specific Tools and Resources
Target Audience: CRCs, CRAs, Investigators, Project Mangers, Regulatory Affairs/Compliance, Medical Monitor, Medical Officer, Project Physician, Quality Assurance, Clinical Research Administrators
Contact hours: 1.0 Contact hours have been approved for through ACRP. Membership is not required for online registration of contact hours.
Contact Hour Cost:
- $0 - Chapter Members
- $15 - ACRP Members
- $30 - Non-Members
To receive contact hours: Purchase the contact hours, sign in at the registration desk and attend the program. Please Log on to the ACRP website then “ACRP Learning Portal” to complete the evaluation no later than 30 days following the event and obtain the online certificate.
Further Information: Leslie Korbee is a Consultant for Clinical and Translational Research at the Office Clinical and Translational Research, Cincinnati Children’s Hospital Medical Center.
#DirectororManagerofRegulatoryAffairs #RegulatoryAffairs #ClinicalResearchCoordinator #StudyandSiteManagement #RegulatorySpecialist