Pharmaceutical industry news
Fresh coverage across pharma, biotech, medtech, research, approvals, and market-moving developments.
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🌍discoverynews.google.comTier 3 · Aggregated media
Taiho Oncology, Inc., Taiho Pharmaceutical Co., Ltd., and Cullinan Therapeutics, Inc. Report Zipalertinib Plus Chemotherapy Meets Primary Endpoint in Phase 3 Rezilient3 Trial in First-Line Egfr Exon 20 Insertion Mutation Non-Small Cell Lung Cancer
marketscreener.comOriginal source
🇺🇸Regulatoryfederalregister.govTier 1 · Regulatory source
Kremers Urban Pharmaceuticals, Inc.; Grant of Hearing Request Regarding a Proposal To Withdraw Approval of an Abbreviated New Drug Application for Extended-Release Methylphenidate Tablets
The Food and Drug Administration (FDA or the Agency) is announcing a formal evidentiary public heari...
Federal RegisterOriginal source
🇺🇸Regulatoryfederalregister.govTier 1 · Regulatory source
Agency Information Collection Activities: Proposed Collection; Public Comment Request: Information Collection Request Title: SAMHSA Data Security Requirements for Accessing Confidential Data (OMB No. 0930-0396)
Substance Abuse and Mental Health Services (SAMHSA), within the Department of Health and Human Servi...
Federal RegisterOriginal source
🇺🇸Regulatoryfederalregister.govTier 1 · Regulatory source
Medicaid Program; Prohibition on Federal Medicaid and Children's Health Insurance Program Funding for Sex-Rejecting Procedures Furnished to Children
This final rule requires that a State Medicaid plan must provide that the Medicaid agency will not m...
Federal RegisterOriginal source
🇺🇸Regulatoryfederalregister.govTier 1 · Regulatory source
Medicare Program; Alternative Payment Model (APM) Incentive Payment Advisory for Clinicians-Request for Current Billing Information for Qualifying APM Participants
This advisory is to alert certain clinicians who are Qualifying Alternative Payment Model (APM) part...
Federal RegisterOriginal source
🇺🇸Regulatoryfederalregister.govTier 1 · Regulatory source
Formal Meetings Between the Food and Drug Administration and Sponsors or Applicants of Prescription Drug User Fee Act Products; Guidance for Industry; Availability
The Food and Drug Administration (FDA or Agency) is announcing the availability of a final guidance...
Federal RegisterOriginal source






