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🇺🇸Regulatoryfederalregister.govTier 1 · Regulatory source

Center for Scientific Review; Amended Notice of Meeting

Federal RegisterOriginal source
🇺🇸Regulatoryfederalregister.govTier 1 · Regulatory source

Importer of Controlled Substances Application: Wedgewood Pharmacy LLC

Wedgewood Pharmacy LLC has applied to be registered as an importer of basic class(es) of controlled...

Federal RegisterOriginal source
🇺🇸Regulatoryfederalregister.govTier 1 · Regulatory source

Importer of Controlled Substances Application: AndersonBrecon, Inc. DBA PCI Pharma Services

AndersonBrecon, Inc. DBA PCI Pharma Services has applied to be registered as an importer of basic cl...

Federal RegisterOriginal source
🇺🇸Regulatoryfederalregister.govTier 1 · Regulatory source

Importer of Controlled Substances Application: Aphena Pharma Solutions MD, LLC

Aphena Pharma Solutions MD, LLC has applied to be registered as an importer of basic class(es) of co...

Federal RegisterOriginal source
🇺🇸Regulatoryfederalregister.govTier 1 · Regulatory source

Importer of Controlled Substances Application: Veranova, L.P.

Veranova, L.P. has applied to be registered as an importer of basic class(es) of controlled substanc...

Federal RegisterOriginal source
🇺🇸Regulatoryfederalregister.govTier 1 · Regulatory source

Importer of Controlled Substances Application: Scottsdale Research Institute

Scottsdale Research Institute has applied to be registered as an importer of basic class(es) of cont...

Federal RegisterOriginal source
🇺🇸Regulatoryfederalregister.govTier 1 · Regulatory source

Importer of Controlled Substances Application: Arizona Department of Corrections

Arizona Department of Corrections has applied to be registered as an importer of basic class(es) of...

Federal RegisterOriginal source
🇺🇸Regulatoryfederalregister.govTier 1 · Regulatory source

Center for Scientific Review; Notice of Closed Meetings

Federal RegisterOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source

Drug recall: PRIMIDONE

Official structured record identifier: 99146.

openFDA Drug RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source

Drug recall: BEEKEEPER'S NATURALS Saline Nasal Spray, Sinus Congestion Rinse, Made with Propolis + Xylitol, 1 FL OZ (30 mL) per bottle, Manufactured For: Beekeeper's Naturals USA Inc., Covina, CA 91723

Official structured record identifier: 99145.

openFDA Drug RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source

Drug recall: MINOCYCLINE HYDROCHLORIDE

Official structured record identifier: 99129.

openFDA Drug RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source

Drug recall: NIACIN

Official structured record identifier: 99127.

openFDA Drug RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source

Drug recall: Gas-X Extra Strength, SIMETHICONE 125 mg/ANTIGAS, packaged in a) 120 SoftGels (UPC 3 00674 35041 9, b) 72 SoftGels (UPC 3 00439 00572 1), Distributed by: Haleon, Warren, NJ 07059.

Official structured record identifier: 99125.

openFDA Drug RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source

Drug recall: BUDESONIDE

Official structured record identifier: 99113.

openFDA Drug RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source

Drug recall: ZEP ALCOHOL SANITIZER

Official structured record identifier: 99112.

openFDA Drug RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source

Drug recall: DULOXETINE

Official structured record identifier: 99108.

openFDA Drug RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source

Drug recall: EPINEPHRINE

Official structured record identifier: 98997.

openFDA Drug RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source

Drug recall: DOXORUBICIN HYDROCHLORIDE

Official structured record identifier: 98921.

openFDA Drug RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source

Device recall: Fresh Roast Systems ColorTrack. Model Name: ColorTrack. Model Number: BENCH R-100

Official structured record identifier: 99111.

openFDA Device RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source

Device recall: Halyard, Towel Six Pack. Kit Code: AMTS70-01.

Official structured record identifier: 99021.

openFDA Device RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source

Device recall: Siemens Dimension Tacrolimus Flex Reagent Cartridge (TAC), REF DF207, SMN 10700795; enzyme immunoassay

Official structured record identifier: 98985.

openFDA Device RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source

Device recall: MOSAIQ Oncology Information System

Official structured record identifier: 98980.

openFDA Device RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source

Device recall: NeoSpan¿ SuperElastic Compression Staple w/Instruments Catalog Number and Product Name T50 SN010 NeoSpan¿ SuperElastic Compression Staple w/Instruments, Size 10x10x10 UDI-DI Code: 00817906020083 T50 SN012 NeoSpan¿ SuperElastic Compression Staple w/Instruments, Size 12x12x12 UDI-DI Cod

Official structured record identifier: 98978.

openFDA Device RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source

Device recall: Boston Scientific Model SC-4318, Clik X Anchor REF: M365SC43180

Official structured record identifier: 98941.

openFDA Device RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source

Device recall: Boston Scientific CSK Electrodes: REF: CSK-TC10, CSK Electrode, STAINLESS STEEL, 10 cm x 28 ga (0.36 mm) REF: CSK-TC10-3M,CSK Electrode, STAINLESS STEEL, 3M Cable, 10 cm x 28 ga (0.36 mm); REF: CSK-TC15, CSK Electrode, STAINLESS STEEL, 15 cm x 28 ga (0.36 mm); REF: CSK-TC15-3M, CSK El

Official structured record identifier: 98939.

openFDA Device RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source

Device recall: SD LTM 64 PLUS, EEG Amplifier/recorder, Model/Catalog Number: SD LTM 64 PLUS, Software Version: firmware 2021.02, 2022.01 or 2022.02

Official structured record identifier: 98924.

openFDA Device RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source

Device recall: Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx40mm Model/Catalog Number: CND0840

Official structured record identifier: 98922.

openFDA Device RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source

Device recall: Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-4320

Official structured record identifier: 98907.

openFDA Device RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source

Device recall: Bicarby Dialysate; Model number: RFP-400-G;

Official structured record identifier: 98892.

openFDA Device RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source

Device recall: Mahurkar Elite PASS Trays; Description (Product Number/CFN): 12 FR x 13cm Acute Dual Lumen Catheter with Straight Extensions, PASS Tray (8888221413), 12 FR x 16cm Acute Dual Lumen Catheter with Curved Extensions, PASS Tray (8888222416), 12 FR x 16cm Acute Dual Lumen Catheter with Stra

Official structured record identifier: 98891.

openFDA Device RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source

Device recall: Allia IGS 3 Pulse angiographic X-ray system

Official structured record identifier: 98880.

openFDA Device RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source

Device recall: Brand Name: EXENT Analyser Product Name: EXENT Analyser Model/Catalog Number: IE800.A Software Version: 1.0.20 Product Description: The EXENT Analyser is an automated analyser intended for the qualitative and quantitative in vitro measurement of analytes in human body fluids used in c

Official structured record identifier: 98830.

openFDA Device RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source

Device recall: NexxZr T Multi A3.5 W98-16mm, REF: 745451

Official structured record identifier: 98823.

openFDA Device RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source

Device recall: TDC VELOCE", 23G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT23, 9311.23G01, 9311.23G02, 9311.23K01, 9311.23K02, 9311.23K03, 9623.G0201, 9623.G0202, 9623.K0201, 9311.23G01-00;

Official structured record identifier: 98814.

openFDA Device RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source

Device recall: Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52 TESTS Product Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52 TESTS Model/Catalog Number: 1023780 Software Version: N/A Product Description: The SporeTraq Mail-In Spore Testing Service includes 52 bacterial Spore Strips provide

Official structured record identifier: 98695.

openFDA Device RecallsOriginal source
🇪🇺Researcheuropepmc.orgTier 2 · Direct publisher

Safety and Effectiveness of Iota-Carrageenan Eye Drops for the Treatment of Dry Eye Disease.

Europe PMCOriginal source
🇪🇺Researcheuropepmc.orgTier 2 · Direct publisher

Basket and umbrella trials in pediatric precision medicine: a systematic review of designs, opportunities, and challenges.

Europe PMCOriginal source
🇪🇺Researcheuropepmc.orgTier 2 · Direct publisher

Cognitive-behavioural therapy for insomnia in adults to decrease cannabis use: study protocol for a randomised controlled trial in a community sample of adults with frequent cannabis use.

Europe PMCOriginal source
🇪🇺Researcheuropepmc.orgTier 2 · Direct publisher

Therapeutic monitoring of beta-lactams in critically ill patients with sepsis: Clinical trial protocol.

Europe PMCOriginal source
🇪🇺Researcheuropepmc.orgTier 2 · Direct publisher

A randomized controlled trial of N-acetylcysteine in the treatment of early-onset preeclampsia: Study Protocol.

Europe PMCOriginal source
🇺🇸CROinvestor.medpace.comTier 2 · Direct publisher

Medpace Holdings, Inc. to Report Second Quarter 2026 Financial Results on July 22, 2026

MedpaceOriginal source
🌍Researchopenclinica.comTier 2 · Direct publisher

What Does a Connected Clinical Trial Workflow Actually Look Like?

OpenClinicaOriginal source
🌍Industrymaravai.comTier 1 · Company source

TriLink Opens GMP Enzyme Manufacturing Facility, Enabling Integrated IVT Supply from R&D to Commercial Scale

Maravai LifeSciencesOriginal source
🌍Medialemsurgical.comTier 2 · Direct publisher

Why a ‘Surgical Robot’ is more than just a ‘Robotic Arm’ and the transition from surgery 2.0 to surgery 3.0

LEM Surgical (Dynamis Spine Robot)Original source
🌍Industrycibeles.com.uyTier 1 · Company source

BUCANER 430F

Cibeles (Uruguay)Original source
🌍Industrycibeles.com.uyTier 1 · Company source

Bucaner 430f

Cibeles (Uruguay)Original source
🌍Industryadial.comTier 1 · Company source

Adial Pharmaceuticals Expands Executive Leadership Team and Closes PIPE Financing

Adial PharmaceuticalsOriginal source
🌍Researchpremier-research.comTier 2 · Direct publisher

FDA’s Drug Repurposing Push Puts 505(b)(2) Strategy in Focus

Premier ResearchOriginal source
🇫🇷Regulatoryleem.orgTier 1 · Regulatory source

INVITATION CONFERENCE DE PRESSE : Résultats 2026 du baromètre 360° de l’attractivité de la France pour l’industrie pharmaceutique

LEEM FranceOriginal source
🇫🇷Researchpresse.inserm.frTier 2 · Direct publisher

CLOVES Syndrome : European Medicines Agency grants marketing authorisation for alpelisib

INSERMOriginal source
🇨🇭CDMOsiegfried.chTier 2 · Direct publisher

Siegfried strengthens manufacturing network with new large-scale drug substance facility in Minden

SiegfriedOriginal source
🇺🇸Regulatoryfda.govTier 1 · Regulatory source

Early Alert: Convenience Kit Issue from Windstone Medical Packaging, Inc.

Certain Cardinal Health Webcol Large Alcohol Prep Pads in Custom Convenience Kits manufactured by Al...

FDA MedWatchOriginal source
🇺🇸Regulatoryfda.govTier 1 · Regulatory source

Disruptions in Availability of Breast Biopsy Needles - Letter to Health Care Providers

The FDA issued a LHCP to notify providers that Stereotactic Breast Biopsy Needles (product code KNW)...

FDA MedWatchOriginal source
🌍Industryamarin.co.thTier 3 · Secondary coverage

งานบ้านและสวนแฟร์ Shopping Week 2026 วันที่ 20 – 28 มิถุนายน 2569 เวลา 10.00 – 21. 00 น. ณ ฮอลล์ 8 – 10 อิมแพ็ค เมืองทองธานี

Amarin CorporationOriginal source
🇺🇸Researchmedicine.yale.eduTier 2 · Direct publisher

Yale School of Medicine

Yale MedicineOriginal source
🇪🇺Researcheuropepmc.orgTier 2 · Direct publisher

Optimal Clinical Trials Platform for Progressive Multiple Sclerosis (OCTOPUS): protocol for an international, multi-arm, multi-stage, platform, randomized controlled, double-blind, phase 3 clinical trial

Europe PMCOriginal source
🇪🇺Researcheuropepmc.orgTier 2 · Direct publisher

Evidence Readiness Assessment for Drug Repurposing Using Data Quality, Safety Signals, Network Structure, and Bayesian Uncertainty

Europe PMCOriginal source
🇪🇺Researcheuropepmc.orgTier 2 · Direct publisher

Semi-automated [68Ga]Ga-FAPI-46 radiosynthesis using GalliAd® generator and MiniAIO® synthesizer: development and validation for PET imaging of fibroblast activation protein

Europe PMCOriginal source
🇪🇺Researcheuropepmc.orgTier 2 · Direct publisher

Effects of Ganoderma lucidum Polysaccharide Peptide on Inflammatory and Metabolic Biomarkers in Obese Patients with Cardiometabolic Syndrome: A Randomized Controlled Trial.

Europe PMCOriginal source
🇪🇺Researcheuropepmc.orgTier 2 · Direct publisher

Changes in remimazolam plasma concentration associated with the Pringle maneuver during hepatectomy: a pilot study.

Europe PMCOriginal source