Welcome to 'Fundamentals of Good Clinical Practice: Recruitment and Trial'! This is the third course in the Clinical Trial GCP series. It is designed to introduce you to the processes, procedures and documentation needed prior, during and after a clinical trial according to Good Clinical Practice (GCP). In Courses One and Two, we explored the foundations of clinical research, including the preparations and documentation needed to begin a trial as well as the role of the investigator, site staff and the IRB/IEC. We conclude our GCP studies with this final course. The course is divided into several modules, each covering specific stages of a clinical trial. The modules include a variety of videos, a fictional case study and interactive quizzes to reinforce your learning. Enroll now and start building a strong foundation in the conduct of clinical research!
The Informed Consent Form
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Skills You'll Learn
Record Keeping, Patient Safety, Patient Education And Counseling, Clinical Research, Healthcare Ethics, Regulatory Compliance, Clinical Trials
Reviews
4.8 (140 ratings)
- 5 stars80.71%
- 4 stars16.42%
- 3 stars2.14%
- 1 star0.71%
MM
May 29, 2025
This course is a combination of videos and readings that offers an easy way to learn the basis of GCP in clinical trials.
BL
May 20, 2025
A very helpful course which helped me for better understanding of Clinical trials and associated Good Laboratory Practices
From the lesson
Patient consent and working with vulnerable subjects
In Week Two, we鈥檒l focus on the consent process, and also discuss what to consider when working with vulnerable patient groups.
Taught By
Novartis Learning