This course is part of Clinical Trials: Good Clinical Practice Specialization

Instructor: Novartis Learning

What you'll learn

  •   Explore the clinical trial process, the details of good clinical practice, and regulatory requirements.

    • Skills you'll gain

  •   Patient Education And Counseling
  •   Record Keeping
  •   Patient Safety
  •   Regulatory Compliance
  •   Healthcare Ethics
  •   Clinical Trials
  •   Clinical Research

    • There are 3 modules in this course

    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!

    Patient consent and working with vulnerable subjects

    Conducting a Clinical Trial

    Explore more from Research

    ©2025  ementorhub.com. All rights reserved