PMDA
Showing 17–25 of 25 results
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PMDA Notification No.171/2004: Procedures for Developing Post-marketing Study Plan
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PMDA PFSB/ELD Notification No.899/2001: Points to Consider for Reducing Total Review Time for New Drug Applications
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PMDA-CPE No.1116002: Procedure for Remote Inspection for Drugs & Regenerative Products
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PMDA-PSEHB-MDED No. 0709-2: Ensuring the Quality and Safety of Gene Therapy Products
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PMDA/PFSB Notification No. 0304004/2009: Guideline for the Quality, Safety, & Efficacy Assurance of Follow-on Biologics
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PMDA: Points to Consider for Reprocessed Single-use Medical Devices
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PSEHB No. 0731-1 : Conditional Early Approval System for Innovative Medical Devil Products (Fast-Break Scheme)
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PSEHB No.0201: Applications for Marketing Approval related to the Period of Transitional Measures with respect to the Handling of Medical Device Software
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YAKUSHOKUKIHATSU No. 0331006/2006: Good Clinical Practices for Medical Devices
$200.00 Add to cart
