Speakers
Laurent Patern Tshimpaka
(Autorité Congolaise de Réglementation Pharmaceutique)
Mariana Roldão Santos
(WHO, Technical Officer, Facilitated Product Introduction)
Naira Romanova
(Scientific Centre of Drug and Medical Technology, Armenia)
Rutendo Kadzunge
(Medicines Control Authority, Zimbabwe)
Rwanda FDA
(Rwanda FDA)
Tanapon Wongkaew
(Thailand Food and Drugs Administration )
Description
Moderator: Victoria Palmi, EMA
- Principles and methodology of CRP
- CRP statistics: by countries and regions and by CRP stream - SRA CRP and PQ CRP (medicines, vaccines, IVDs)
- National regulatory authorities’ experiences: numbers and types of products, timelines, experiences, recommendations
Short presentations/interventions from each of the speaker (5 minutes max) followed by Q&A and discussion
