Regulated Product Submission
The charter of this working group is to build on the common Table of Contents for medical device regulatory submissions and create a dynamic template that supports the electronic transmission of regulatory submissions.
The charter of this working group is to build on the common Table of Contents for medical device regulatory submissions and create a dynamic template that supports the electronic transmission of regulatory submissions.
Chile - Public Health Institute of Chile (ISP)
Chinese Taipei Taiwan Food and Drug Administration (TFDA)
Cuba - Centro para el Control Estatal de Medicamentos, Equipos y Dispositivos Médicos (CECMED)
Egypt - Egyptian Drug Authority (EDA)
Israel - The Medical Technology, Health Information, Innovation and Research Directorate (MTIIR)
Montenegro - Institute for Medicine and Medical Devices of Montenegro (CINMED)
Nigeria - National Agency for Food and Drug Administration Control (NAFDAC)
South Africa - South African Health Products Regulatory Authority (SAHPRA)