Our Accelerated CRP Course is designed only for professionals who already have some experience in the clinical research field. It covers many of the same topics as CRP2.0, but more in-depth, and without some introductory concepts. Our Placement Assistance Til Hired (PATH) program is also included, providing students with the tools to find and obtain employment within this industry.
To verify your eligibility to this course, email a request to do the Admission test at firstname.lastname@example.org
This course covers the following topics:
- US Regulations and the FDA
- Canadian and International Regulations Ethics Review Boards
- Informed Consent
- Adverse Events
- Study Design
- Essential Documents
- Site Evaluation and Selection
- Site Initiation
- Monitoring Visits
- Study Close Out
- Data Management
- Information Privacy
- Electronic Data
- Data and Safety Monitoring Board
N.B.: This program is only for GCP trained and experienced professionals.
Before enrolling, you must pass a test of your GCP knowledge to assess your eligibility.
Email a request to get the Admission test to email@example.com