Type
Course
WHO Good Reliance Practices
Emplacement
En ligne
Durée
1 Heures
Zone du programme
Other
Site internet
Prix
0.00 $US
Personne de référence de l'évenement
globalhealth@unitar.org
Inscription
Événement en inscription ouverte
Mode de livraison
Formation en ligne
Langue (s)
Anglais
Pilier
NCD Digital Health and Capacity Building
Objectifs de l'événement
- Explain what reliance is;
- State the main principles of reliance;
- Describe the key concepts and general considerations for reliance;
- Recognize how reliance can be used for the regulatory oversight of medical products; and
- Identify challenges and opportunities for reliance.
Arrière plan
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.
Contenu et structure
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:
- build regulatory capacity in Member States consistent with good regulatory practices;
- promote regulatory cooperation, convergence and transparency through networking, work-sharing and reliance.
Reliance is an effective way of regulating medical products through using global resources more efficiently.
The course will:
- introduce WHO Good Reliance Practices (GRelP);
- outline the main principles of reliance;
- advocate for the use of reliance in the regulatory oversight of medical products; and
- promote the good reliance principles.
Méthodologie
Approximate course duration: 35 minutes (additional time might be needed for the test)
Languages
This course is available in the following languages: Français, Español
Content Warning
This course may contain images, videos, and multimedia materials related to healthcare that may include graphic depictions of medical conditions, surgical procedures, and other clinical content. These materials are intended for educational purposes to enhance understanding of real-world medical scenarios and are essential for the comprehensive learning experience.
Viewer discretion is advised. If you find any content distressing, you may pause or skip the material as needed.
Audience visée
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.
Informations supplémentaires
Assessment & Awards
You will receive a Confirmation of Participation upon completing all the modules in this course. Please note that this award does not serve as a professional qualification.
Other information
Guidance note
The content of this course has been validated, verified, and is owned by WHO Regulatory Convergence and Networks, Regulation and Safety Unit.
This course is not a WHO Academy co-produced course. In case of any concerns or feedback on the course content, please share your feedback in the survey form at the end of this course.
Browser and device compatibility
For the best experience, we recommend using the latest version of Chrome, Firefox, Safari, or Microsoft Edge to access the courses.
Produced by: WHO Regulatory Convergence and Networks, Regulation and Safety Unit.
Protection des données et confidentialité
Les données personnelles des participant·e·s qui postulent, s’inscrivent ou participent aux formations et autres événements de l’UNITAR sont régies par la Politique de protection des données et de confidentialité. En postulant, en s’inscrivant ou en participant à cet événement, le ou la participant·e reconnaît avoir pris connaissance de cette politique et en accepter les conditions.