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- Total Review Period for Standard Products Reduced by 4.5 Months to 14.7 Months: PMDA
July 18, 2011
- Positive PII Results for Takeda's TAK-875 Presented at ADA
July 18, 2011
- Ryukaikon Calls For Further Studies on Bar Code Labeling
July 18, 2011
- Committee Starts Discussing Relief System for Victims of Health Hazards Caused by Anticancer Drugs
July 18, 2011
- Positive Results for Central Neuropathic Pain with Lyrica in PIII Trial: Pfizer
July 18, 2011
- SymBio Licenses Rigosertib from Onconova for MDS
July 18, 2011
- Takeda Recalls Actos, Competact in France
July 18, 2011
- Combined with Insulin, Lixisenatide Decreases HbA1c
July 18, 2011
- Hisamitsu to Launch Norspan Tape in Early August Aiming for ¥1.3 Bil. Sales in FY2011
July 18, 2011
- Senju Files for Glaucoma Treatment Seen as Next-generation Strategic Product
July 18, 2011
- Eisai to Accelerate Biomarker Research with Its Subsidiary EIDIA
July 18, 2011
- Roche Returns Overseas Development, Marketing Rights for SGLT-2 Inhibitor to Chugai
July 18, 2011
- Pancreatic Cancer Approved as Add'l Indication for Tarceva: Chugai
July 18, 2011
- DPC Subcommittee to Look at Fixed-sum Reimbursement per Hospitalization for High-priced Drugs
July 18, 2011
- Further Consolidation of Dispensing Pharmacies Expected: Mr Ubunuki of Yano Research
July 18, 2011
- GSK Obtains Marketing Approval for Rotarix
July 18, 2011
- Taisei Kako Co-develops New Prefilled Syringe with Suzuken
July 18, 2011
- Kyowa Kirin to Enforce Safe Driver Education for New MRs
July 18, 2011
- 3 Products Including 4-Valent HPV Vaccine Gardasil Approved: MSD
July 18, 2011
- Nippon Kayaku Takes over Manufacturing Approval for Gelpart from Astellas
July 18, 2011
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