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calendar

14,106 catalysts · 3,350 8k filing · 2,402 grant · 2,299 approval · 1,631 device 510k · 1,179 device recall · 1,115 device pma

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  • 8k filing3,350
  • grant2,402
  • approval2,299
  • device 510k1,631
  • device recall1,179
  • device pma1,115
device adverse event
1,000
  • earnings584
  • recall465
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Oct 20, 2025

    2
    ›Oct 25, 2025approval295d agoCARBON DIOXIDE, USP (CARBON DIOXIDE) — FDA approval

    Sponsor: ROBERTS OXYGEN CO INC. Form: GAS. Route: INHALATION

    full page →fda approvals ↗
    ›Oct 25, 2025device recall295d agoFresenius Medical Care Holdings, Inc. device recall (Cls II)Fresenius Medical Care AG

    5008X CAREsystem +CLiC +CDX; — Reason: Several software anomalies with the potential to impact patient treatment, of which one includes the possibility to result in treatment stop if certain conditions are fulfilled. — Status: Ongoing

    full page →fda device recalls ↗

    Week of Oct 27, 2025

    48
    ›Oct 27, 2025approval293d agoTRAMADOL HYDROCHLORIDE — FDA approvalTrigen Laboratories Inc

    Sponsor: PLIVA. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Oct 27, 2025approval
    ← prev
    page 15 of 283
    next →
    293d ago
    OPDIVO QVANTIG (NIVOLUMAB) — FDA approval(hyaluronidase (recombinant, human) + nivolumab)

    Sponsor: BRISTOL-MYERS SQUIBB. Form: INJECTABLE. Route: SUBCUTANEOUS

    full page →(hyaluronidase (recombinant, human) + nivolumab) →fda approvals ↗
    ›Oct 27, 2025approval293d agoOPDIVO QVANTIG (NIVOLUMAB) — FDA approval(hyaluronidase (recombinant, human) + nivolumab)

    Sponsor: BRISTOL-MYERS SQUIBB. Form: INJECTABLE. Route: SUBCUTANEOUS

    full page →(hyaluronidase (recombinant, human) + nivolumab) →fda approvals ↗
    ›Oct 27, 2025approval293d agoLOMUSTINE — FDA approvalLOMUSTINE

    Sponsor: CARNEGIE. Form: CAPSULE. Route: ORAL

    full page →LOMUSTINE →fda approvals ↗
    ›Oct 27, 2025approval293d agoGLYCOPYRROLATE — FDA approvalFresenius Kabi USA LLC

    Sponsor: AJENAT PHARMS. Form: SOLUTION. Route: ORAL

    full page →fda approvals ↗
    ›Oct 27, 2025approval293d agoCOLUMVI (GLOFITAMAB-GXBM) — FDA approvalglofitamab

    Sponsor: GENENTECH INC. Form: INJECTABLE. Route: INJECTION

    full page →glofitamab →fda approvals ↗
    ›Oct 27, 2025approval293d agoDUREZOL (DIFLUPREDNATE) — FDA approvalDIFLUPREDNATE

    Sponsor: SANDOZ. Form: EMULSION. Route: OPHTHALMIC

    full page →DIFLUPREDNATE →fda approvals ↗
    ›Oct 27, 2025approval293d agoPOTASSIUM CHLORIDE — FDA approvalTWi Pharmaceuticals Inc

    Sponsor: TWI PHARMS. Form: TABLET, EXTENDED RELEASE. Route: ORAL

    full page →fda approvals ↗
    ›Oct 27, 2025approval293d agoSEVELAMER CARBONATE — FDA approvalRenvela

    Sponsor: NAVINTA LLC. Form: TABLET. Route: ORAL

    full page →Renvela →fda approvals ↗
    ›Oct 27, 2025approval293d agoASTEPRO ALLERGY (AZELASTINE HYDROCHLORIDE) — FDA approvalWallace Pharmaceuticals Inc

    Sponsor: BAYER HLTHCARE. Form: SPRAY, METERED. Route: NASAL

    full page →fda approvals ↗
    ›Oct 27, 2025approval293d agoKINERET (ANAKINRA) — FDA approvalSobi Inc

    Sponsor: BIOVITRUM AB. Form: VIAL. Route: SUBCUTANEOUS

    full page →fda approvals ↗
    ›Oct 27, 2025device 510k293d agoCircle Cardiovascular Imaging, Inc. — cvi42 Coronary Plaque Software Application (510k cleared)

    Product code: QIH. Advisory committee: Radiology. Type: Traditional

    full page →fda device 510k ↗
    ›Oct 27, 2025device 510k293d agoPatriot Laser, LLC — Patriot Duo (510k cleared)

    Product code: GEX. Advisory committee: General, Plastic Surgery. Type: Traditional

    full page →fda device 510k ↗
    ›Oct 27, 2025device 510k293d agoShenzhen Jamr Technology Co., Ltd. — Blood Pressure Monitor (B73, BE23T) (510k cleared)Fortior Technology (Shenzhen) Co., Ltd./ADR

    Product code: DXN. Advisory committee: Cardiovascular. Type: Traditional

    full page →fda device 510k ↗
    ›Oct 27, 2025device 510k293d agoOsteocentric Technologies, Inc. — OsteoCentric Navigated Instruments System (510k cleared)

    Product code: OLO. Advisory committee: Neurology. Type: Traditional

    full page →fda device 510k ↗
    ›Oct 27, 2025device 510k293d agoTouchbeauty Beauty & Health ( Shenzhen ) Co., Ltd — VITA Multi-Function Head Brush (TB-2443F, TB-2442AF, TB-2343F, TB-2442F) (510k cleared)

    Product code: OHS. Advisory committee: General, Plastic Surgery. Type: Traditional

    full page →fda device 510k ↗
    ›Oct 27, 2025device 510k293d agoTechfit Digital Surgery, Inc. — TECHFIT Patient-Specific Cranial System (510k cleared)

    Product code: GWO. Advisory committee: Neurology. Type: Traditional

    full page →fda device 510k ↗
    ›Oct 27, 2025device 510k293d agoFimilla (Shanghai) Maternity & Baby Articles Co., Ltd. — Electric Breast Pump (HL-3058, F5112) (510k cleared)

    Product code: HGX. Advisory committee: Obstetrics/Gynecology. Type: Traditional

    full page →fda device 510k ↗
    ›Oct 27, 2025device 510k293d agoViet Phu Trade and Import Export Co., Ltd. — Disposable Vinyl Examination Gloves (510k cleared)

    Product code: LYZ. Advisory committee: General Hospital. Type: Traditional

    full page →fda device 510k ↗
    ›Oct 27, 2025device 510k293d agoAffinity Biosensors, LLC — LifeScale Gram Negative Kit (LSGN) with the LifeScale AST system (510k cleared)

    Product code: SAN. Advisory committee: Microbiology. Type: Traditional

    full page →fda device 510k ↗
    ›Oct 27, 2025device 510k293d agoFimilla (Shanghai) Maternity & Baby Articles Co., Ltd. — Electric Breast Pump (HL-3060, F5113) (510k cleared)

    Product code: HGX. Advisory committee: Obstetrics/Gynecology. Type: Traditional

    full page →fda device 510k ↗
    ›Oct 27, 2025device pma293d agoW. L. Gore & Associates, Inc. — GORE® VIATORR® TIPS Endoprosthesis with Controlled Expansion (PMA supplement)

    Supplement type: Normal 180 Day Track. Product code: MIR. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Oct 27, 2025device pma293d agoBoston Scientific Corp — ROTAPRO™ Rotational Atherectomy System (PMA supplement)BOSTON SCIENTIFIC CORP

    Supplement type: 30-Day Notice. Product code: MCX. Advisory committee: CV. Decision: OK30

    full page →fda device pma ↗
    ›Oct 27, 2025device pma293d agoEdwards Lifesciences, LLC — TRIFORMIS RESILIA Tricuspid Valve (PMA supplement)Edwards Lifesciences Corp

    Supplement type: Panel Track. Product code: LWR. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Oct 27, 2025device recall293d agoMedline Industries, LP device recall (Cls II)

    Quick Strip Fabric Sterile Adhesive Bandages, 1" x 3", Medline Item Number NON25660QS — Reason: Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 27, 2025device recall293d agoMedline Industries, LP device recall (Cls II)

    Quick Strip Fabric Sterile Adhesive Bandages, 0.75" x 3", Medline Item Number NON25650QS — Reason: Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 27, 2025device recall293d agoMedline Industries, LP device recall (Cls II)

    Quick Strip Plastic Sterile Adhesive Bandages, 0.75" x 3", Medline Item Number NON25500QS — Reason: Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 27, 2025device recall293d agoMedline Industries, LP device recall (Cls II)

    Fur Friends Plastic Sterile Adhesive Bandages, 0.75" x 3", Medline Item Number NON256133QS — Reason: Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 27, 2025device recall293d agoPhilips North America device recall (Cls II)

    Azurion R3.0. Model Number 722234. Commercial Name: Azurion 7 M20. INTERVENTIONAL FLUOROSCOPIC XRAY SYSTEM — Reason: Between July 2024 and June 2025, Philips Azurion R3.0 systems with a FlexArm stand were shipped without the Source-to-Skin Distance (SSD) Spacer. The SSD spacer is necessary to meet the FDA minimum source-skin distance requirement of 38 cm for standard fluoroscopy applications. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 27, 2025device recall293d agoMedline Industries, LP device recall (Cls II)

    CURAD Germ-Shield Touch-Free Fabric Bandages, Sterile, 0.75" x 3", 30/Box, Medline Item Number CUR1930F — Reason: Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 27, 2025device recall293d agoMedline Industries, LP device recall (Cls II)

    Curad Quick Strip Fabric Bandages Containing 30 Bandages of 3/4" x 3", Medline Item Number CUR1930P — Reason: Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 27, 2025device recall293d agoMedline Industries, LP device recall (Cls II)

    MEDLINE PERFUSION SYRINGE, REF: DYNJ39223C — Reason: Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing BD Luer Tip Caps. BD has issued a recall of their Luer Tip Caps after confirming through internal testing that certain BD Luer Tip Cap trays failed routine biocompatibility testing. Although the tip cap covers a small surface area of the syringe and does not come in direct contact with patients, there is the potential that the failure of a biocompatibility test may have varying consequences ranging from no harm or clinical impact to potential for sensitization, irritation, pyrogenicity, acute systemic toxicity or hemolysis depending on the nature and duration of contact with the syringe. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 27, 2025device recall293d agoNipro Medical Corporation device recall (Cls II)

    Hemodialysis System, Surdial DX REF: MC+SDX01 Rx Only — Reason: Screw may loosen or fallout of Hemodialysis system — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 27, 2025device recall293d agoMedline Industries, LP device recall (Cls II)

    Quick Strip Plastic Sterile Adhesive Bandages, 1" x 3", Medline Item Number NON25600QS — Reason: Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 28, 2025approval292d agoTICAGRELOR — FDA approvalTICAGRELOR

    Sponsor: APOTEX. Form: TABLET. Route: ORAL

    full page →TICAGRELOR →fda approvals ↗
    ›Oct 28, 2025approval292d agoTICAGRELOR — FDA approvalTICAGRELOR

    Sponsor: MSN. Form: TABLET. Route: ORAL

    full page →TICAGRELOR →fda approvals ↗
    ›Oct 28, 2025approval292d agoENLON-PLUS (ATROPINE SULFATE) — FDA approvalAccord Healthcare Inc

    Sponsor: PHARMOBEDIENT. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    ›Oct 28, 2025approval292d agoTRIUMEQ (ABACAVIR SULFATE) — FDA approvalViiV Healthcare Company

    Sponsor: VIIV HLTHCARE. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Oct 28, 2025approval292d agoENLON-PLUS (ATROPINE SULFATE) — FDA approvalAccord Healthcare Inc

    Sponsor: PHARMOBEDIENT. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    ›Oct 28, 2025approval292d agoEBGLYSS (LEBRIKIZUMAB-LBKZ) — FDA approvallebrikizumab

    Sponsor: ELI LILLY AND CO. Form: INJECTABLE. Route: INJECTION

    full page →lebrikizumab →fda approvals ↗
    ›Oct 28, 2025approval292d agoTIVICAY (DOLUTEGRAVIR SODIUM) — FDA approvalViiV Healthcare Company

    Sponsor: VIIV HLTHCARE. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Oct 28, 2025approval292d agoDEXTROAMPHETAMINE SULFATE — FDA approvalDEXTROAMPHETAMINE SULFATE

    Sponsor: AZURITY. Form: TABLET. Route: ORAL

    full page →DEXTROAMPHETAMINE SULFATE →fda approvals ↗
    ›Oct 28, 2025approval292d agoTICAGRELOR — FDA approvalAstraZeneca Pharmaceuticals LP

    Sponsor: CHANGZHOU PHARM. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Oct 28, 2025approval292d agoTICAGRELOR — FDA approvalSciegen Pharmaceuticals Inc

    Sponsor: SCIEGEN PHARMS. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Oct 28, 2025approval292d agoTICAGRELOR — FDA approvalAstraZeneca Pharmaceuticals LP

    Sponsor: TARO. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Oct 28, 2025approval292d agoNICARDIPINE HYDROCHLORIDE — FDA approvalAmneal Pharmaceuticals, Inc.

    Sponsor: QILU PHARM HAINAN. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    ›Oct 28, 2025approval292d agoRENFLEXIS (INFLIXIMAB-ABDA) — FDA approvalinfliximab biosimilar

    Sponsor: SAMSUNG BIOEPIS CO LTD. Form: INJECTABLE. Route: INJECTION

    full page →infliximab biosimilar →fda approvals ↗
    ›Oct 28, 2025approval292d agoTIVICAY PD (DOLUTEGRAVIR SODIUM) — FDA approvalViiV Healthcare Company

    Sponsor: VIIV HLTHCARE. Form: TABLET, FOR SUSPENSION. Route: ORAL

    full page →fda approvals ↗
    $FMS23.77+0.59%
    $FRTRY
    $BMY63.83-1.27%
    $BMY63.83-1.27%
    $LLY1180.16-2.25%
    $BSX51.83+0.27%
    $EW91.33-2.47%
    $AMRX18.15+5.10%