The Ministry of Health, Labor and Welfare (MHLW) on December 12 presented a draft outline of the FY2026 drug pricing…
REGULATORY
PMDA Plans to Introduce Full Scale “Patient ADR Reporting System” by FY2018
The Pharmaceuticals and Medical Devices Agency (PMDA) plans to introduce a full-scale system for receiving reports of adverse drug reactions (ADRs) directly from patients by FY2018, the final year of its third midterm plan. A patient ADR reporting system was…
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Japan has presented its latest draft policy direction for its FY2026 drug pricing reform. While the package includes a string…
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