Research Ethics and Good Clinical Practice

Current Status
Not Enrolled
Price
Free
Get Started

Course Description:

“Research Ethics and Good Clinical Practice (GCP)” dives into the foundational principles and practices essential for conducting ethical medical and health research. This course navigates the historical, ethical, and practical aspects of research, offering insights into the roles and responsibilities of key stakeholders, from investigators to sponsors. With a special focus on the Cameroonian context, participants will gain a comprehensive understanding of the ethical review landscape, informed consent processes, and the intricacies of study design and protocol development.

Course Objectives:

  • Equip participants with a robust understanding of research ethics and Good Clinical Practice (GCP).
  • Highlight the significance of ethical considerations in medical and health research.
  • Provide insights into the roles and responsibilities of investigators, sponsors, and ethics review boards.
  • Offer a deep dive into the Cameroonian ethics review landscape and its relevance in global research contexts.
  • Foster an understanding of the informed consent process, emphasizing participant autonomy and rights.
  • Encourage the application of ethical principles in real-world research scenarios.

Course by:

Instructors

This course is delivered by the ethics team of CRENC-IeDEA under the guidance of Prof Anastase Dzudie.

Gabriel Mabou

Gabriel Mabou

MPH

Bonaventure Dzekem

Dr. Ebasone Peter Vanes

MD, PhD

Anastase Dzudie

Prof. Anastase Dzudie

MD, PhD, FESC, ASR

Certificate Awarded

Earn a Certificate upon completion

Beginner Level

Suitable for starters

Completely Online

Start instantly at your own schedule

In English

Only available in English for now

Course Content

Expand All
Lesson Content
0% Complete 0/2 Steps

8 thoughts on “Research Ethics and Good Clinical Practice”

  1. As a result ethics i now know that before i collect consent in need to identify the vulnerable population.
    I now know there is an aspect like risk-benefits assessments, i also know about transparency in terms of open communication and data sharing.
    I also know about the principles that guide research designs and practices
    As a result of ethics, i also took notice of information form.
    As a result of Good Clinical Practice i now have a great insight on designing, conducting, recording and reporting clinical trials that involve people

  2. Thank you so much to the trainers and the team as a whole.
    Certificate downloaded successfully.
    I’m very grateful for the knowledge I’ve gained from this course.
    It is already shaping me into a better researcher.
    Thanks again!

Leave a Reply

Your email address will not be published. Required fields are marked *

Never Miss a Thing!

Never Miss a Thing!

Subscribe to our mailing list to receive the latest news and updates on our webinars, articles and courses.

You have Successfully Subscribed!