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!
HG
This course is amazing in its simple yet comprehensive way in touching all important aspects in a concise manner, with link to further reading for details. Thank you so much Novartis
MM
This course is a combination of videos and readings that offers an easy way to learn the basis of GCP in clinical trials.
CR
Although had a good knowledge this did brush up my GCP skills
NS
Very informative! Information was presented in a concise and engaging format. I really enjoyed the course. It was well done.
CW
This is a great overview of a clinical trial & GCP.
BL
A very helpful course which helped me for better understanding of Clinical trials and associated Good Laboratory Practices
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This course is amazing in its simple yet comprehensive way in touching all important aspects in a concise manner, with link to further reading for details. Thank you so much Novartis
What I liked about the course is that there were many case studies, it was very human/patient focused, not just about ICH guidelines. However, I do not understand why I cannot receive a course certificate during the free trial week.
An excellent overview of ICH GCP for the non-expert who wants a basic understanding of how it works in the pharmaceutical world. It doesn't cover ISO 14155 (medical devices) but a lot of the same basic principles apply. I appreciate that part of the ICH GCP document were provided. My one piece of feedback to the organizers is that some of the FDA guidance documents that the course links to (e.g., clinical trial diversity plans) have now been taken down from the FDA site per EO of the new administration.
Very engaging and informative for someone new to the industry. Loved the simple graphic of the video content. The concepts were conveyed in a very clear manner. Loved the sections reviewing the essential and the central trial documents and close-out process as well as audits nd inspections.
Very informative! Information was presented in a concise and engaging format. I really enjoyed the course. It was well done.
A very helpful course which helped me for better understanding of Clinical trials and associated Good Laboratory Practices
This course is a combination of videos and readings that offers an easy way to learn the basis of GCP in clinical trials.
Very easy to follow, clear and concise information. Very useful for understanding clinical trials
El material está bien explicado e ilustrado, hay ejemplos para mejor compresión.
Although had a good knowledge this did brush up my GCP skills
excellent, it has all the basic information.
Enjoyable course. Content well explained
Great course I enjoyed learning
Really informative and complete
Thank you for the opportunity.
Outstanding learning process!
This course is very useful
Very interesting course
Very informative!
very informative