Robust and well-functioning Quality Management System (QMS) is a key enabler of the Good Regulatory Practices (GRP) for National Regulatory Authorities (NRAs) of medical products. A quality management system, which includes application of quality risk management principles, makes the decisions of regulatory authorities more credible and their operations more stable and consistent.
In response to Members States requests, WHO developed and recently published three guidance documents to help NRA’s establish and implement QMS.
Join us for a Live webinar to launch the WHO QMS guidance documents, including experience from two regulators (ANVISA of Brazil and MCAZ of Zimbabwe) on their journey along with challenges towards QMS implementation.
Live interpretation into Arabic, French, Russian and Spanish languages will be provided.
To register please click HERE