|Duration: 2 hours (the average time to complete the training program, including final assessments).
Credits Hours: 2
Self-paced Training: 24/7 access to course.
Enrollment Period: 3 months.
Demonstration: Try one of our FREE courses.
Certificate: View sample certificate.
THIS COURSE IS CURRENTLY NOT AVAILABLE.
Contact the BioPharma Institute for more information.
Training Program: GCP: Clinical Trial Monitoring: Site Evaluation and Set-up
Training Provided By: BioPharma Institute
Availability: Immediately available upon ordering.
Description: Online training with immediate access upon enrollment. The purpose of site evaluation and set-up is to ensure that the site has access to the required patient population, has appropriately qualified staff, adequate time and facilities to conduct the study and to ensure the site is fully prepared for the conduct of the clinical trial. This online course provides an understanding of the training requirements for clinical research associates (CRAs), including familiarization with study documentation. The procedures necessary prior to initiation of an investigational site, particularly the site qualification visit, are described in detail. The responsibilities and procedures associated with preparing for and conducting initiation visits are also covered in detail.
Certification Requirements: Students must view the entire program and successfully pass an online, multiple-choice final assessment with >80% passing grade within a 90 day period of time (180 days for Professional Certification Programs). Certificate is accessible in PDF format immediately after satisfying requirements.
Online Training Programs Include:
The GCP: Clinical Trial Monitoring: Site Evaluation and Set-up course is found in the following professional certification program(s):
Students completing this course should be able to: Describe the evaluation and qualification process at an investigational site. Identify the study documentation required prior to commencing work on a clinical trial. Describe what is required of a study site to conduct a clinical trial successfully. Outline the procedures to be conducted prior to the initiation of a study site. Describe the measures taken during site evaluation, set-up and initiation to ensure that the conduct of clinical trials complies with the protocol. Describe the initiation process at an investigational site.
For more information on the BioPharma Institute’s training programs, or to suggest a course, please complete the form located below. Alternatively, you may call toll free in the US: (888) 4-BIO-LRN, international callers can dial (201) 301-8370, or email Support@BioPharmaInstitute.com.