The aim of this course is to provide an introduction to WHO Good Reliance Practices (GRelP) and to advocate for the use of reliance in the regulatory oversight of medical products. It is intended for staff from National Regulatory Authorities and all relevant stakeholders interested in using reliance.
Please note: These materials were launched on 26/10/2022
This course is also available in the following languages:
Strong regulatory systems for medical products are a critical element of well-functioning health systems and important contributors to improving access, and ultimately achieving universal health coverage. The objectives of WHO in the area of regulatory system strengthening are to:
Reliance is an effective way of regulating medical products through using global resources more efficiently.
The course will:
The course is primarily designed for staff from National Regulatory Authorities. It is also intended for all stakeholders involved – including those from industry, academia, governments, and policy makers.
Approximately 30 minutes.
A Record of Achievement certificate will be available to participants who score at least 80% in the final assessment. Participants who receive a Record of Achievement can also download an Open Badge for this course. Click here to learn how.