Certificate in Clinical Trials

This exam checks your understanding of how clinical trials are planned, conducted, and reviewed. It covers trial phases, ethics, regulations, team roles, and data handling.

This exam is useful for students in life sciences or pharmacy, clinical trial assistants, nurses, and professionals working in the pharmaceutical, biotech, or healthcare sectors.

No. Anyone with a basic background in biology, health sciences, or an interest in clinical research can take this exam.

It includes clinical trial design, trial phases, participant safety, ethics, informed consent, regulatory guidelines, data collection, and global research trends.

Yes. This exam helps you understand key clinical research processes and prepares you for entry-level roles or further certifications in the field.

Yes. The exam includes content based on Good Clinical Practice (GCP) and International Council for Harmonisation (ICH) standards.

Yes. You will learn about all stages of clinical trials, from early testing to post-marketing surveillance, and how drugs move through these phases.

Yes. Nurses, pharmacists, and other healthcare staff involved in patient trials or studies will benefit from understanding how clinical trials operate.

Yes. After passing the exam, you will receive a certificate that shows your knowledge of clinical trial practices. This can be added to your resume or job applications.

Yes. It is a good first step for those planning to pursue certifications such as ACRP, SOCRA, or GCP-based clinical research programs.