Japan’s Ministry of Health, Labor and Welfare (MHLW) on March 5 unveiled the revised NHI prices for drugs subject to…
REGULATORY
PMDA Considering Review Procedure Policy for IVD Agents Based on FDA Guidance Draft
Regarding ongoing requirements to enhance the review system for in vitro diagnostic (IVD) agents aimed at promoting personalized healthcare, Pharmaceuticals and Medical Devices Agency (PMDA) Deputy Review Director Daisei Miyamoto (Office of Medical Devices II) revealed at a lecture held…
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