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PMDA continues to improve the public health and safety of our nation by reviewing applications for marketing approval of pharmaceuticals and medical devices, conducting safety measures, and providing relief to people who have suffered from adverse drug reactions.
Message from the Chief Executive
The Pharmaceuticals and Medical Devices Agency (PMDA) focuses on three key areas: relief services for adverse health effects, product reviews, and post-marketing safety measures. These three encompass the entire life cycle of drugs and medical devices from development through to the postmarketing period.
Outline of PMDA
Mid-term Targets / Mid-term Plan
PMDA International Vision
PMDA International Strategic Plan