Good Clinical Practice (GCP) – Self Assessment Exam

VALIDATE YOUR KNOWLEDGE AS A SUCCESSFUL CLINICAL TRIAL EXPERT ON ICH E6 GOOD CLINICAL PRACTICE (GCP) GUIDELINE

GCP SELF-ASSESSMENT EXAM

This is an exam based on best choice questions. It is designed not only for giving provision to investigators and site staff but also the assessment is important for CRAs, Clinical QA, Regulatory Affairs departments and Clinical Operations staff. This exam will empower professionals, whether presently taking part in clinical research or looking to get involved as a prospective career. It will help to self assess their knowledge on GCP roles and how to manage a GCP compliance clinical trial. The learners will be assessed on following important areas of GCP:

•GCP Terminologies

•GCP Principles

•Informed consent

•Investigation products

•Trial specific documentation

•Data integrity key principles

•Dos and Donts of GCP

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Food for Thought

Be Familiar with ICH GCP E6 (R2) knowledge which you hold…

If you think you are an expert in ICH GCP E6 (R2) after taking courses on the subject and working with it…

You need to hold on!

Join this exam and self-assess yourself!

Maybe you need to learn and learn…

Or you can prove your knowledge and expertise by completing this exam.

Both ways, you are in a win-win situation.

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Certification:Udemy does not provide certification for exams; they only do in the case of Video Courses. But the great news here is, we have empowered our paid students to have a certificate once they qualify by 80% in the exams. It is a manual process in which learners are requested to submit evidence of qualification and apply for the certificate. The certificates are issued at the end of a month.

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THIS SELF ASSESSMENT GCP COURSE WILL HELP YOU TO:

• Confirm you comprehension on the key ICH-GCP requirements and regulatory expectations regarding conduct of clinical trials

• Confirm that you know the responsibilities of an investigator/ investigator team within clinical trials

• Verify your understanding why, when and how clinical trial activities are to be conducted and documented

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