HOME > Discussions on Next PMD Act Amendment
Discussions on Next PMD Act Amendment
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Quality Assurance and Lag/Loss Fight to Form Pillars of PMD Act Amendment
December 27, 2024
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Japan to Require Drug Makers to Set Up Legal Post of “Stable Supply Manager”
November 29, 2024
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Advisory Panel Backs Transfer of GMP Inspection Authority for New Generics to PMDA
November 5, 2024
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Panel OKs Withdrawal Rule for Conditional Nod, 2-Year Extension for Pediatric Data Protection towards PMD Act Amendment
October 4, 2024
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MHLW Lays Out Updated Discussion Timeline for PMD Act Amendment
September 13, 2024
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MHLW Mulls System to Seek Expert Input for Patent Linkage
July 29, 2024
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Panelists Wary of Proposed Switch of Generic GMP Inspection Authority to PMDA
July 8, 2024
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Make Onsite GMP Inspections Mandatory for Patented Meds and New Generics: MHLW Proposal
June 10, 2024
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MHLW Proposes Creating Legal Provision on RWD-Only Drug Submissions
June 10, 2024
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Japan Eyes Withdrawal Rule for Conditional Approval, More Flexible Nods
June 10, 2024
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JPA Wary of FPMAJ Pitch to Allow Non-Pharmacists as Drug Production Managers
May 21, 2024
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Allow Use of OOS Autologous Cell Products via PMD Act Amendment: FIRM
May 21, 2024
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Pharma Industry Wants “Internationally Harmonized” Rules under PMD Act
May 20, 2024
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MHLW Panel Sets Topics for PMD Act Amendment; Pediatrics, Drug Loss on Agenda
April 19, 2024
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