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
MPH
Dr. Ebasone Peter Vanes
MD, PhD
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
Very grateful for this wonderful platform which just permitted me to gather enough knowledge as for as research is concerned. Thanks so much to the team
Good morning everyone, thanks for giving me this awesome opportunity. I can’t wait to commerce this program
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
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!
Interested, can’t wait to begin
Good learning experience
The course was quite enriching, when are we expecting the certificate, or it is ready for download. thanks