Japan’s Ministry of Health, Labor and Welfare (MHLW) on March 5 unveiled the revised NHI prices for drugs subject to…
REGULATORY
PMDA to Promote Simplification of Documentation Required in Applications, Acceptance of Documents in Electronic Form
The Pharmaceuticals and Medical Devices Agency (PMDA) plans to ramp up its initiative to promote the simplification of documents required in applications for marketing authorization and its acceptance of application documents in electronic form. The PMDA announced its plan on…
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