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REGULATORY
- Harvoni, Sovaldi under Review for Risks of Hypertension, Cerebrovascular Disorder
June 13, 2016
- MHLW to Set Up Subcommittee to Help Implement AMR Action Plan
June 13, 2016
- AMED to Establish New Scheme to Support Commercialization of Drug Seeds from Academia
June 10, 2016
- MHLW to Revise Guidelines on Use of Blood Products
June 10, 2016
- Upcoming ICH Meeting Expected to Approve New Members Including Generic Drug Organization
June 9, 2016
- Company Funding for AMED-Backed Clinical Research Also Subject to Legal Regulation: Govt
June 8, 2016
- Use of MID-NET in PMS Could Promote Comparisons of One’s Own Products with Other Treatments: FPMAJ Official
June 7, 2016
- MHLW to Place 2-Year Grace Period on Mandatory Barcode Labeling by March 2021 for Companies with “Special Circumstances”
June 6, 2016
- 141 Trials of Nucleic Acid Drugs Underway Worldwide, but 70% Being Conducted by US Companies: JPO Survey
June 6, 2016
- Cabinet OKs New Growth Strategy, Basic Economic and Fiscal Policy
June 3, 2016
- “Minor Discrepancies” between Marketing Approval and Actual Manufacturing Processes Found for about 70% of Products: MHLW
June 3, 2016
- Clinical Research Bill Didn’t Clear Diet, Now under Continued Review
June 2, 2016
- Tax Hike Delay Kills Feared Price Cuts in 2017, but Concerns Linger over Expensive Drug Debate
June 2, 2016
- MHLW Proposes Discontinuing Supply of Human Thrombin Products
June 2, 2016
- MHLW Expects Stable Supply of Kaketsuken’s Blood Products Despite Earthquake Damage: Official
June 2, 2016
- Bisphosphonate Labels to Add Osteonecrosis of External Auditory Canal in ADR List
June 1, 2016
- Boehringer’s Reversal Agent for Pradaxa Becomes 1st Drug Subject to Japan’s Compassionate Use Scheme
June 1, 2016
- MHLW Initiates Discussions on Palliative Care for CV Diseases
June 1, 2016
- MHLW Drug Review Panel Shelves ASKA’s Hepatic Encephalopathy Drug
May 31, 2016
- Lawmakers Eye Genomic Medicine Bill to Fuel Diagnostics Development
May 31, 2016
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