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calendar

120 catalysts · 33 grant · 29 approval · 25 device recall · 16 recall · 10 device 510k · 7 device pma

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no tagged catalysts yet

Week of Sep 29, 2025

50
›Oct 1, 2025device 510k317d agoVisby Medical, Inc. — Visby Medical Men's Sexual Health Test (510k cleared)Vivani Medical, Inc.

Product code: QEP. Advisory committee: Microbiology. Type: Dual Track

full page →fda device 510k ↗
›Oct 1, 2025device 510k317d agoShenzhen Ulike Smart Electronics Co., Ltd. — Jmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG) (510k cleared)

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

full page →fda device 510k ↗
›Oct 1, 2025device 510k317d agoHebei Newangie Technology Co., Ltd. — Picosecond laser device (BMPS4) (510k cleared)

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

full page →fda device 510k ↗
›Oct 1, 2025device 510k317d agoWuxi Hisky Medical Technologies Co., Ltd. — Shear Wave Quantificational Ultrasound Diagnostic System (FH9000/FH7000/FH6000/FH5000/FH3000/FH1000) (510k cleared)

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

full page →fda device 510k ↗
›Oct 1, 2025device 510k317d agoNewclip Technics — Newclip Patient-matched instrumentation non sterile PSI (510k cleared)

Product code: PBF. Advisory committee: Orthopedic. Type: Traditional

full page →fda device 510k ↗
›Oct 1, 2025device pma317d agoAbiomed, Inc. — Impella 5.5 with SmartAssist (PMA supplement)Abion Inc

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

full page →fda device pma ↗
›Oct 1, 2025device pma317d agoBiotronik, Inc. — Ilivia 7 VR-T DX; Intica 7 VR-T DX; Intica 5 VR-T DX; Ilivia 7 VR-T; Ilivia 7 DF4 VR-T; Intica 7 VR-T; Intica 7 DF4 VR-T (PMA supplement)

Supplement type: Special (Immediate Track). Product code: LWS. Advisory committee: CV. Decision: APPR

full page →fda device pma ↗
›Oct 1, 2025device pma317d agoKARL STORZ Endoscopy-America, Inc. — Photodynamic Diagnostic D-Light C System (PMA supplement)

Supplement type: 30-Day Notice. Product code: OAY. Advisory committee: GU. Decision: OK30

full page →fda device pma ↗
›Oct 1, 2025device pma317d agoBiotronik, Inc. — Ilivia Neo 7 DR-T; Intica Neo 7 DR-T; Intica Neo 5 DR-T (PMA supplement)

Supplement type: Special (Immediate Track). Product code: MRM. Advisory committee: CV. Decision: APPR

full page →fda device pma ↗
›Oct 1, 2025device pma317d agoBiotronik, Inc. — Ilivia Neo 7 VR-T DX; Ilivia Neo 7 VR-T; Intica Neo 7 VR-T DX; Intica Neo 7 VR-T; Intica Neo 5 VR-T DX; Intica Neo 5 VR- (PMA supplement)

Supplement type: Special (Immediate Track). Product code: LWS. Advisory committee: CV. Decision: APPR

full page →fda device pma ↗
›Oct 1, 2025device pma317d agoBiotronik, Inc. — Edora 8 DR-T; Evity 8 DR-T; Enitra 8 DR-T; Enticos 8 DR-T; Evity 6 DR-T; Enitra 6 DR-T; Edora 8 DR; Enitra 6 DR; Edora 8 (PMA supplement)

Supplement type: Special (Immediate Track). Product code: NVZ. Advisory committee: CV. Decision: APPR

full page →fda device pma ↗
›Oct 1, 2025device pma317d agoRayner Intraocular Lenses , Ltd. — Rayner C-flex 570C, C-flex Aspheric 970C, 600C Aspheric, RayOne Aspheric RAO600C, RayOne Spheric RAO100C and RayOne EMV (PMA supplement)

Supplement type: 30-Day Notice. Product code: HQL. Advisory committee: OP. Decision: OK30

full page →fda device pma ↗
›Oct 1, 2025device recall317d agoPhilips Medical Systems DMC GmbH device recall (Cls II)

Radiography 7300 C; Model Number: 712037; — Reason: Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/physical exertion required for manual movement) due to potential manufacturing issues. — Status: Ongoing

full page →fda device recalls ↗
›Oct 1, 2025device recall317d agoMedline Industries, LP device recall (Cls II)

Medline Renewal LigaSure Blunt Tip Sealer/Divider, Compatible with FT10 Generator, 5 mm x 37 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed — Reason: Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodged. — Status: Ongoing

full page →fda device recalls ↗
›Oct 1, 2025device recall317d agoMedline Industries, LP device recall (Cls II)

Medline Renewal Ligasure Impact Sealer/Divider NanoCoated, Compatible with FT10 Generator 18cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed — Reason: Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodged. — Status: Ongoing

full page →fda device recalls ↗
›Oct 1, 2025device recall317d agoPhilips Medical Systems DMC GmbH device recall (Cls II)

DigitalDiagnost C90 (1) High Performance, (2) Flex/Value/Chest/ER; Model Number: (1) 712034, (2) 712035; — Reason: Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/physical exertion required for manual movement) due to potential manufacturing issues. — Status: Ongoing

full page →fda device recalls ↗
›Oct 1, 2025device recall317d agoENDOMAGNETICS LTD device recall (Cls II)

Magseed Pro 12 cm soft tissue marker. Model Number: MS2-17-1-12. Product Description: The Endomag Magseed Pro Magnetic Marker System is a sterile, single use device composed of a marker preloaded in a 17ga Needle Delivery System. The Endomag Magseed Pro Marker is indicated for use to radiographically mark soft tissue during a surgical procedure or for future surgical procedures. — Reason: Potential for contamination with cotton fibers. — Status: Ongoing

full page →fda device recalls ↗
›Oct 1, 2025device recall317d agoMedline Industries, LP device recall (Cls II)

Medline Renewal LigaSure Small Jaw Instrument (Purple/White), Compatible with FT10 Generator 18.8 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed — Reason: Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodged. — Status: Ongoing

full page →fda device recalls ↗
›Oct 1, 2025device recall317d agoMedline Industries, LP device recall (Cls II)

Medline Renewal Ligasure Blunt Tip Sealer/Divider NanoCoated, Compatible with FT10 Generator 44cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed — Reason: Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodged. — Status: Ongoing

full page →fda device recalls ↗
›Oct 1, 2025device recall317d agoPhilips Medical Systems DMC GmbH device recall (Cls II)

Precision CRF; Model Number: 706400; — Reason: Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/physical exertion required for manual movement) due to potential manufacturing issues. — Status: Ongoing

full page →fda device recalls ↗
›Oct 1, 2025device recall317d agoMedline Industries, LP device recall (Cls II)

Medline Renewal Ligasure Maryland Jaw Sealer/Divider NanoCoated, Compatible with FT10 Generator 44 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed — Reason: Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodged. — Status: Ongoing

full page →fda device recalls ↗
›Oct 1, 2025device recall317d agoAbiomed, Inc. device recall (Cls I)Abion Inc

Automated Impella Controller (AIC), used for left heart support blood pump, labeled as the following with corresponding Product Codes: 1. Impella Controller, Packaged, AU; Product Code: 0042-0000-AU. 2. Impella Controller, Packaged, CA; Product Code: 0042-0000-CA. 3. Impella Controller, Packaged, EU; Product Code: 0042-0000-EU. 4. Impella Controller, Packaged, EU, Loaner; Product Code: 0042-0000-EU-L. 5. Impella Controller, Packaged, IN; Product Code: 0042-0000-IN. 6. Impella Controller, Packaged, JP; Product Code: 0042-0000-JP. 7. Impella Controller, Japan, Loaner; Product Code: 0042-0000-JP-L. 8. Impella Controller, Packaged, UK; Product Code: 0042-0000-UK. 9. Impella Controller, UK, Loaner; Product Code: 0042-0000-UK-L. 10. Impella Controller, Packaged, US; Product Code: 0042-0000-US. 11. Impella Controller, Packaged, US, Loaner; Product Code: 0042-0000-US-L. 12. Impella Optical Controller, Packaged, AU; Product Code: 0042-0010-AU. 13. Impella Optical Controller, Packaged, EU; Product Code: 0042-0010-EU. 14. Impella Optical Controller, EU, Loaner; Product Code: 0042-0010-EU-L. 15. Impella Optical Controller, Packaged, IN; Product Code: 0042-0010-IN. 16. Impella Optical Controller, Packaged, UK; Product Code: 0042-0010-UK. 17. Impella Optical Controller, UK, Loaner; Product Code: 0042-0010-UK-L. 18. Impella Optical Controller, Packaged, US; Product Code: 0042-0010-US. 19. Impella Optical Controller, US, Loaner; Product Code: 0042-0010-US-L. 20. Optical, AIC, Impella Connect, Pkgd, AU; Product Code: 0042-0040-AU. 21. Optical AIC w/Impella Connect,Pack'd, CA; Product Code: 0042-0040-CA. 22. AIC w/Remote Link, Pkgd, Cln Trl, US; Product Code: 0042-0040-CT. 23. AIC w/Remote Link, Pkgd, Cln Trl, US; Product Code: 0042-0040-CT-L. 24. Optical AIC w/Impella Connect,Pack'd, EU; Product Code: 0042-0040-EU. 25. Optical AIC w/Impella Connect,EU,Loaner; Product Code: 0042-0040-EU-L. 26. Optical AIC w/Impella Connect, Pkgd, JP; Product Code: 0042-0040-JP. 27. Optical AIC w/Impella Connect, Pkgd, JP; Product Code: 0042-0040-JP-L. 28. Optical, AIC, Impella Connect, Pkgd, UK; Product Code: 0042-0040-UK. 29. Optical, AIC, Impella Connect, Pkgd, US; Product Code: 0042-0040-US. 30. Optical AIC Impella Connect, US, Loaner; Product Code: 0042-0040-US-L. 31. Dbl optical, AIC Impella Connect, Phg US; Product Code: 1000201. 32. AIC w/Impella Connect for ECP; Product Code: 1000432. — Reason: Potential cybersecurity vulnerabilities related to the operating system in the Automated Impella Controller (AIC). — Status: Ongoing

›Oct 1, 2025device recall317d agoBeckman Coulter, Inc. device recall (Cls II)

Beckman Coulter UniCel DxI 600, Part Numbers: A71460, A30260; Photometric Chemistry Analyzer — Reason: An internal investigation has determined that due to defective sub-components within the gantry assembly, a z-axis CAD movement motion error may occur and cause an analyzer to enter a Not Ready or Paused state, leading to a delay in obtaining results. — Status: Ongoing

full page →fda device recalls ↗
›Oct 1, 2025device recall317d agoMedline Industries, LP device recall (Cls II)

Medline Renewal Ligasure Blunt Tip Sealer/Divider NanoCoated, Compatible with FT10 Generator 37 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed — Reason: Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodged. — Status: Ongoing

full page →fda device recalls ↗
›Oct 1, 2025device recall317d agoQuest International, Inc. device recall (Cls II)QDM International Inc.

Brand Name: ReQuest Measles IgG Product Name: Rubeola IgG Enzyme Linked Immunoabsorbant Assay Model/Catalog Number: 01-190 Software Version: N/A Product Description: Measles IgG tests, performed using ELISA (Enzyme-Linked Immunosorbent Assay) method, used to detect the presence of IgG antibodies against measles virus in a patient's serum or plasma Component: not a component — Reason: Due to distributing the measles IgG IVD without a premarket approved/cleared. — Status: Ongoing

full page →fda device recalls ↗
›Oct 1, 2025device recall317d agoPhilips Medical Systems DMC GmbH device recall (Cls II)

ProxiDiagnost N90; Model Number: 706110; — Reason: Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/physical exertion required for manual movement) due to potential manufacturing issues. — Status: Ongoing

full page →fda device recalls ↗
›Oct 1, 2025device recall317d agoMedline Industries, LP device recall (Cls II)

Medline RenewalLigasure Blunt Tip Sealer/Divider, NanoCoated Compatible with FT10 Generator 23 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed — Reason: Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodged. — Status: Ongoing

full page →fda device recalls ↗
›Oct 1, 2025device recall317d agoPhilips Medical Systems DMC GmbH device recall (Cls II)

CombiDiagnost R90; Model Number: 709031; — Reason: Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/physical exertion required for manual movement) due to potential manufacturing issues. — Status: Ongoing

full page →fda device recalls ↗
›Oct 1, 2025device recall317d agoMedline Industries, LP device recall (Cls II)

Medline Renewal LigaSure Exact, Dissector without Nano-Coating 21cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical Cutting And Coagulation Device — Reason: Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodged. — Status: Ongoing

full page →fda device recalls ↗
›Oct 1, 2025device recall317d agoMedline Industries, LP device recall (Cls II)

Medline Renewal LigaSure Impact Curved Large Jaw Sealer/Divider, Compatible with FT10 Generator, FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed — Reason: Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodged. — Status: Ongoing

full page →fda device recalls ↗
›Oct 1, 2025device recall317d agoMicrogenics Corporation device recall (Cls II)

Thermo scientific MAS Omni CARDIO, Liquid Assayed Integrated Cardiac Control, Model/Catalog Number: OCRD-L, OCRD-101, OCRD-202, OCRD-303, OCRD-SP, OCRD-MP, OCRD-UL; Product Description: In Vitro Diagnostic external control — Reason: The firm received complaints from customers reporting vial-to-vial variability when using the control with high sensitivity Troponin I assays. This defect may lead to as delay in patient results for hs Troponin I assays. — Status: Ongoing

full page →fda device recalls ↗
›Oct 1, 2025device recall317d agoMedline Industries, LP device recall (Cls II)

Medline Renewal LigaSure Maryland Jaw Sealer/Divider NanoCoated, Compatible w/FT10 37 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed — Reason: Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodged. — Status: Ongoing

full page →fda device recalls ↗
›Oct 1, 2025device recall317d agoENDOMAGNETICS LTD device recall (Cls II)

Magseed Pro 7 cm soft tissue marker. Model Number: MS2-17-1-07. Product Description: The Endomag Magseed Pro Magnetic Marker System is a sterile, single use device composed of a marker preloaded in a 17ga Needle Delivery System. The Endomag Magseed Pro Marker is indicated for use to radiographically mark soft tissue during a surgical procedure or for future surgical procedures. — Reason: Potential for contamination with cotton fibers. — Status: Ongoing

full page →fda device recalls ↗
›Oct 1, 2025device recall317d agoBeckman Coulter, Inc. device recall (Cls II)

Beckman Coulter UniCel DxI 800, Part Numbers: 973100, A71456; Photometric Chemistry Analyzer — Reason: An internal investigation has determined that due to defective sub-components within the gantry assembly, a z-axis CAD movement motion error may occur and cause an analyzer to enter a Not Ready or Paused state, leading to a delay in obtaining results. — Status: Ongoing

full page →fda device recalls ↗
›Oct 1, 2025device recall317d agoSiemens Medical Solutions USA, Inc device recall (Cls I)

MAGNETOM Cima.X Upgrade. Model Number: 11689304. — Reason: There is a potential for an ice blockage to form or currently exist within the primary and/or the auxiliary venting paths of the magnet helium containment venting system. In the event of a quench when both venting paths are blocked, helium gas may be unable to escape through the designed venting paths, leading to a pressure build-up within the helium containment system. This pressure build-up could ultimately rupture the helium containment system, potentially resulting in a helium leak into the scanning room. — Status: Ongoing

full page →fda device recalls ↗
›Oct 1, 2025device recall317d agoMedline Industries, LP device recall (Cls II)

Medline Renewal LigaSure Maryland Jaw Sealer/Divider Nano Coated, Compatible with FT10 Generator 23 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed — Reason: Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodged. — Status: Ongoing

full page →fda device recalls ↗
›Oct 1, 2025device recall317d agoPhilips Medical Systems DMC GmbH device recall (Cls II)

DigitalDiagnost 4 (1) High Performance, (2) Flex/Value; Model Number: (1) 712031, (2) 712032; — Reason: Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/physical exertion required for manual movement) due to potential manufacturing issues. — Status: Ongoing

full page →fda device recalls ↗
›Oct 1, 2025grant317d agoRLR VA MEDICAL CENTER — Boosting employment to improve health and recovery among Veterans in substanc...

VA grant. PI: Alan Benjamin McGuire

full page →nih reporter ↗
›Oct 1, 2025grant317d agoLOUIS STOKES CLEVELAND VA MEDICAL CENTER — Ancestry-Specific Genetic Influences and Potential Therapeutics for Ocular Di...

VA grant. PI: NEAL S. PEACHEY

full page →nih reporter ↗
›Oct 1, 2025grant317d agoVA PUGET SOUND HEALTHCARE SYSTEM — Determining Optimal Foot Shape Capture Methods to Prioritize Offloading in An...

VA grant. PI: Brittney C Muir

full page →nih reporter ↗
›Oct 1, 2025grant317d agoLOUIS STOKES CLEVELAND VA MEDICAL CENTER — Optimizing deep brain stimulation to improve visuomotor function in Parkinson...

VA grant. PI: Aasef G Shaikh

full page →nih reporter ↗
›Oct 1, 2025grant317d agoVETERANS HEALTH ADMINISTRATION — Mapping Phenotypes in Abdominal Aortic Aneurysms

VA grant. PI: JOHN A CURCI

full page →nih reporter ↗
›Oct 1, 2025grant317d agoVA SAN DIEGO HEALTHCARE SYSTEM — “Neural Stem Cells for Spinal Cord Injury: Studies leading to an IND”

VA grant. PI: MARK H. TUSZYNSKI

full page →nih reporter ↗
›Oct 1, 2025grant317d agoFLORIDA STATE UNIVERSITY — Experimental evaluation of the mechanisms driving acute stress potentiation o...

DA grant. $150,505. PI: Richard Macatee

full page →nih reporter ↗
›Oct 1, 2025grant317d agoVETERANS HEALTH ADMINISTRATION — Testing the Impact of Measurement-Based Care on Quality of Life and DiseaseMa...

VA grant. PI: Shirley Ann Cohen-Mekelburg

full page →nih reporter ↗
›Oct 1, 2025grant317d agoVETERANS ADMIN PALO ALTO HEALTH CARE SYS — A Mobile Health Intervention to Improve Psychosocial Functioning in Veterans ...

VA grant. PI: Haijing Wu Hallenbeck

full page →nih reporter ↗
›Oct 1, 2025grant317d agoWHITE RIVER JUNCTION VA MEDICAL CENTER — Suicide prevention in Department of Veterans Affairs community care network m...

VA grant. PI: Natalie Riblet

full page →nih reporter ↗
›Oct 1, 2025grant317d agoVA NORTHERN CALIFORNIA HEALTH CARE SYS — Driving Simulator Training to Improve Driving Performance in Veteran Stroke P...

VA grant. PI: Juliana V. Baldo

full page →nih reporter ↗
›Oct 1, 2025grant317d agoVA MEDICAL CENTER — Virtual Care Consortium of Research (VC CORE) - COR-20-199

VA grant. PI: Timothy Patrick Hogan

full page →nih reporter ↗
›Oct 1, 2025grant317d agoVETERANS HEALTH ADMINISTRATION — iTBS Therapy for Alleviating Cognitive Deficits after Traumatic Brain Injury

VA grant. PI: Nicole Michelle Weston

full page →nih reporter ↗
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