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REGULATORY
- Japan Weighs Adoption of EMA Approach for Nitrosamine Impurities Risk Assessment
July 14, 2023
- Japan Govt to Stockpile Xofluza for 1.44 Million People
July 14, 2023
- Chuikyo OKs CEA Organization’s Reform Directions for FY2024
July 13, 2023
- Chuikyo Reps Want More Data from Industry to Review Launch Premiums
July 13, 2023
- Chuikyo Discusses Price Maintenance Premium, Focus Is on Company Criteria
July 13, 2023
- Chuikyo Split over Drug Lags and Losses, Rapid Introduction Evaluation System
July 13, 2023
- MHLW Certifies Antibiotics Supply Assurance Plans from Meiji, Fujifilm, Otsuka
July 12, 2023
- MHLW Panel OKs 172 More Health Damage Claims for COVID Vaccines
July 12, 2023
- MHLW Presents Plan to Expand Orphan Drug Designation by Clarifying Requirements
July 11, 2023
- Boost PMDA Manpower to Respond to Proposed Orphan Revamp: Panelists
July 11, 2023
- MHLW Proposes Simultaneous Preparation of Drug Development Plans for Adults and Children
July 11, 2023
- MHLW Pharma Regulation Panel Kicks Off, Agrees to Discuss Incentives to Develop Pediatric Drugs
July 11, 2023
- Label Expansions for Jakavi, Soliris Up for MHLW Panel Review on July 24
July 11, 2023
- PMDA US Office to Set Out Solution for Drug Lag, Loss: Agency Chief
July 10, 2023
- Amid High Turnover Rate, JPWA Presses for New System to Support Drug Prices
July 7, 2023
- Industry Stresses Stronger Price Support Rule to Ensure Stable Supplies
July 7, 2023
- Japan Appropriately Reviewing Alzheimer’s Med Lecanemab: Minister
July 7, 2023
- Reflect Societal Values in Pricing of Regenerative Medicines: FIRM
July 7, 2023
- JPMA Pushes Simple Price Maintenance for Innovative Meds; PhRMA, EFPIA in Sync
July 6, 2023
- Pharma Groups Float New Methods to Evaluate Innovative Drugs for 2024 Reform
July 6, 2023
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