Description
After a person has consented to participate in a study, it is imperative that their study visits take place according to the schedule in the study protocol. This ensures compliance with research regulations and ensures that study procedures are conducted at the correct timepoints. In turn, this maximizes participant safety, minimizes risk, and ensures data integrity.
This course will teach you how to execute a subject visit from scheduling, to visit preparation, to conducting the visit and collecting subject data.
Attendance at this program has been approved for 0.50 contact hours of research specific continuing education on applications for Maintenance of ACRP’s CCRC®, CCRA®, CPI®, or ACRP-CP® certification designations.
The Society of Clinical Research Associates (SOCRA - www.SOCRA.org) accepts documentation of candidate participation in continuing education programs for recertification if the program is applicable to clinical research regulations, operations or management, or to the candidate’s clinical research therapeutic area. This program offers 0.50 hours of CE credit.
Objectives
By the end of this course, learners will be able to:
- Know how to schedule a subject visit.
- Prepare questionnaires, investigational product, and other materials needed for subject visits.
- Understand data collection compliance.
- Understand how to conduct the visit and interact with subjects.
Certificate
By completing/passing this course, you will attain the certificate (No Expiration) Advarra Completion Certificate
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