Analysis of individual placements across 43 companies over the past 18 months paints a vivid picture of Japan’s evolving healthcare industry. This comprehensive snapshot illuminates current market demands, strategic shifts, and the enduring appeal of this pivotal Asian market.Rare Diseases…
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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