Achieving Successful Regulatory Compliance in Clinical Research Trials
Mandy White, M.S.
Supervisor Regulatory Affairs
Cook Children’s Health Care System, Research Administration Office
This program is designed to assist the learner to achieve successful regulatory compliance in clinical trials.
The level of this presentation is CoreUpon Completion of this session, participants should be able to:
- Understand the Concept of Clinical Research Trials
- Learn the Roles and Responsibilities of a Clinical Investigator
- Achieve FDA Regulatory Compliance
Membership is not required for online registration.Cost to attend:
- 5:30 pm Networking & Hors d’oeuvres
- 6:00 pm – 8:00 PM Presentation
There is no cost to attend this presentation.Contact Hour Cost:
- $0 Chapter Members
- $15 ACRP Members
- $30 Non-Members
Anyone working in or pursuing a career in clinical research ACRP Contact Hours:
2.0 Contact hours have been approved for through ACRPTo receive contact hours:
Purchase the contact hours, sign in at the registration desk, and attend the program. Log on to ACRP website then click “ACRP Learning Portal” to complete the evaluation between 1-30 days following the event and receive the online certificate. Sponsors: Scottish Rite Hospital
has provided the room for this event.Medix Clinical Research
will be providing light appetizers. Medix partners with research sites, Sponsors and CROs across the United States to be a resource in workforce solutions. The Medix team can help to provide strategic solutions to recruit and retain top talent in order to drive your quality trials on time and under budget.
The sponsors named above do not have any influence on the content of the presentation.Contact NorthTexas@acrpnet.org
with questions or concerns.