Speaker Profile

BIOGRAPHY

Nyasha Maregere is a consultant in the Special Access Programme (formerly the Facilitated Product Introduction Team) within the Regulation and Safety Unit at WHO Headquarters.
She provides technical support for the implementation of reliance mechanisms, particularly the Collaborative Registration Procedure for medicines approved by WHO-listed authorities (previously stringent regulatory authorities), as well as global health procedures for the approval of medical products.

Nyasha has over 13 years of experience in medicines regulation and international development, having held roles as a pharmaceutical quality assessor and pharmacovigilance officer at the Medicines Control Authority of Zimbabwe, as manager for medicines registration at the Botswana Medicines Regulatory Authority and at GIZ SADC/Botswana as a technical advisor for a project focused on pharmaceutical value chain promotion across the SADC region.
Nyasha holds a Bachelor of Pharmacy (Honours) and a Master of Clinical Pharmacology.