Japan’s Ministry of Health, Labor and Welfare (MHLW) on March 5 unveiled the revised NHI prices for drugs subject to…
REGULATORY
Applications Based on the Revised PAL to Be Accepted from Nov. 25
The Pharmaceuticals and Medical Devices Agency (PMDA) announced on its website on October 14 that it will accept marketing authorization applications and applications for GMP inspections based on the Pharmaceuticals and Medical Devices Law starting November 25. Since the three…
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