PharmaRadar360

PharmaRadar360

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Pharmaceutical industry news

Fresh coverage across pharma, biotech, medtech, research, approvals, and market-moving developments.

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馃實discoverynews.google.comTier 3 路 Aggregated media

Sex offender, a fugitive for 21 years, hid in plain sight as a yacht-owning L.A. biopharma exec

Los Angeles TimesOriginal source
馃實discoverynews.google.comTier 3 路 Aggregated media

Is Krystal Biotech (KRYS) Overvalued On Its KB801 Patent Data Update?

simplywall.stOriginal source
馃實discoverynews.google.comTier 3 路 Aggregated media

The AI Ebb Gives Way to Biotech as Winners Emerge in the U.S. IPO Market

NAI500Original source
馃實discoverynews.google.comTier 3 路 Aggregated media

BIO Asia-Taiwan 2026 Unites 60 Countries, Showcasing Taiwan as a Global Biotech Innovation Partner

PR NewswireOriginal source
馃實discoverynews.google.comTier 3 路 Aggregated media

Trump announces 100% tariffs on imported generic pharmaceutical drugs

France 24Original source
馃實discoverynews.google.comTier 3 路 Aggregated media

MSD advances Korea-linked eye drug, starts four phase 3 trials vs Eylea - CHOSUNBIZ

ChosunbizOriginal source
馃實discoverynews.google.comTier 3 路 Aggregated media

Trump plans generic drug tariffs from 2028 with two-year delay testing U.S. onshoring push

CNBCOriginal source
馃實discoverynews.google.comTier 3 路 Aggregated media

Radiopharm (ASX:RAD) Advances RAD101 and RAD204 with Positive Clinical Trial Updates

Kalkine MediaOriginal source
馃實discoverynews.google.comTier 3 路 Aggregated media

Is Your Allergy Medicine Safe? FDA Recalls Antihistamine Tablets Over Life-Threatening Contamination Concerns

Health and MeOriginal source
馃實discoverynews.google.comTier 3 路 Aggregated media

Shapiro administration launches $125M fund for biotech startups

AudacyOriginal source
馃實discoverynews.google.comTier 3 路 Aggregated media

Trump Plans to Impose Tariffs on Generic Drugs

The New York TimesOriginal source
馃實discoverynews.google.comTier 3 路 Aggregated media

Trump says he will impose tariffs on generic drugs starting in August 2028

PoliticoOriginal source
馃實discoverynews.google.comTier 3 路 Aggregated media

Kolon TissueGene plunges again as US phase 3 for arthritis therapy fails - CHOSUNBIZ

ChosunbizOriginal source
馃實discoverynews.google.comTier 3 路 Aggregated media

AriBio to present AR1001 phase 3 results at CTAD 2026 in Boston

koreabiomed.comOriginal source
馃嚫馃嚘Regulatorysfda.gov.saTier 1 路 Regulatory source

SFDA Grants Orphan Drug Designation to Gritgen Therapeutics for PKU Treatment

The Saudi Food and Drug Authority (SFDA) has granted orphan drug designation to Gritgen Therapeutics...

SFDA Saudi ArabiaOriginal source
馃嚭馃嚫Regulatorysec.govTier 1 路 Regulatory source

GSK filed Form 6-K

SEC EDGAROriginal source
馃嚭馃嚫Regulatoryfederalregister.govTier 1 路 Regulatory source

Submission for Office of Management and Budget Review; Generic for Administration for Children and Families Program Monitoring Activities

The Administration for Children and Families (ACF) intends to request from the Office of Management...

Federal RegisterOriginal source
馃嚭馃嚫Regulatoryfederalregister.govTier 1 路 Regulatory source

Determination That RASUVO (Methotrexate) Solution, 27.5 Milligrams/0.55 Milliliter (27.5 Milligrams/0.55 Milliliter), Was Not Withdrawn From Sale for Reasons of Safety or Effectiveness

The Food and Drug Administration (FDA, Agency, or we) has determined that RASUVO (methotrexate) solu...

Federal RegisterOriginal source
馃嚭馃嚫Regulatoryfederalregister.govTier 1 路 Regulatory source

Center for Scientific Review; Notice of Closed Meetings

Federal RegisterOriginal source
馃嚭馃嚫Regulatoryfederalregister.govTier 1 路 Regulatory source

Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Premarket Notifications Submission

The Food and Drug Administration (FDA) is announcing that a proposed collection of information has b...

Federal RegisterOriginal source
馃嚭馃嚫Regulatoryfederalregister.govTier 1 路 Regulatory source

Agency Information Collection Activities: Proposed Collection: Public Comment Request; Information Collection Request Title: Advanced Nursing Education Program Specific Form OMB No. 0906-0089-Revision

In compliance with the requirement for opportunity for public comment on proposed data collection pr...

Federal RegisterOriginal source
馃嚭馃嚫Regulatoryfederalregister.govTier 1 路 Regulatory source

Bulk Manufacturer of Controlled Substances Application: Cerilliant Corporation

Cerilliant Corporation has applied to be registered as a bulk manufacturer of basic class(es) of con...

Federal RegisterOriginal source
馃嚝馃嚪Devicesessilorluxottica.comTier 1 路 Company source

EssilorLuxottica Expands its Readers Offering with New FGX Brand Partnerships

EssilorLuxotticaOriginal source
馃實Industrybbbiotech.chTier 1 路 Company source

24 Feb, 2026EXPERT COMMENTARYFrom innovation to value realization: The biotech market in a new phaseFind out more

After several years characterized by elevated capital costs, valuation pressure and pronounced risk...

BB BiotechOriginal source
馃嚝馃嚪Industryvalneva.comTier 1 路 Company source

Valneva to Report First Half 2026 Consolidated Financial Results on August 13, 2026

ValnevaOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Drug label update: Baclofen

Official structured record identifier: 3047613d-006b-4011-b5fe-098588f474aa.

openFDA Drug LabelsOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Drug label update: Metronidazole

Official structured record identifier: 2f7d84d4-1085-4243-be88-442eecb85205.

openFDA Drug LabelsOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Drug label update: ondansetron

Official structured record identifier: 2edc0788-dc38-4d21-ba8e-71f159e2d3b1.

openFDA Drug LabelsOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Drug label update: Gentle Laxative

Official structured record identifier: 29c2efc4-d297-46a0-8008-7a2fad9e8b88.

openFDA Drug LabelsOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Drug label update: Metolazone

Official structured record identifier: 27ab833e-b809-4a80-b7fc-b3599f1751d3.

openFDA Drug LabelsOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Drug label update: First Aid Antiseptic

Official structured record identifier: 262ea2c8-f571-1c0b-e063-6394a90af20b.

openFDA Drug LabelsOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Drug label update: First Aid A and D

Official structured record identifier: 25a319d0-d39a-5ff0-e063-6394a90a671d.

openFDA Drug LabelsOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Drug label update: Baby Vitamin A and D

Official structured record identifier: 25a125ea-6f9f-310c-e063-6394a90acef2.

openFDA Drug LabelsOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Drug label update: Moisture Barrier

Official structured record identifier: 258f3392-0f42-21e8-e063-6294a90ae9ad.

openFDA Drug LabelsOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Drug label update: Heat Pain Relief

Official structured record identifier: 2434f9cf-74aa-17af-e063-6294a90a56d9.

openFDA Drug LabelsOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Drug label update: Cooling Pain Relief

Official structured record identifier: 24345ccf-c96f-31b0-e063-6294a90a82b5.

openFDA Drug LabelsOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Drug label update: Numbing Pain Relief

Official structured record identifier: 2425badb-e196-e9f8-e063-6294a90a7bf4.

openFDA Drug LabelsOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Drug label update: Icosapent

Official structured record identifier: 1aca884c-c464-900d-ac06-33aee7118df8.

openFDA Drug LabelsOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Drug label update: KeepGoing Non Sting Cleaning Wipe

Official structured record identifier: 1a6303ce-8df7-4e8b-93f2-e162fdd2540c.

openFDA Drug LabelsOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Drug label update: fluconazole

Official structured record identifier: 16b6fba0-b96f-4252-a70d-31dc61400298.

openFDA Drug LabelsOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Drug label update: Aripiprazole

Official structured record identifier: 119e3387-39a2-4fe5-904b-c2d008425c0a.

openFDA Drug LabelsOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Drug label update: unspecified product

Official structured record identifier: 0aeb5de1-07f2-4b3e-bd87-ac054e53ccf3.

openFDA Drug LabelsOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Drug label update: Vicks PainQuil PAIN RELIEVER

Official structured record identifier: 0ad7b313-5d72-4cc0-97f0-1a30770350af.

openFDA Drug LabelsOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Drug label update: Cold and Flu Nighttime

Official structured record identifier: 0ab2ba6a-1fac-4a34-ab76-0b50b425d0ba.

openFDA Drug LabelsOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Drug label update: Dove

Official structured record identifier: 00eef191-4eaa-5b06-e063-6294a90ad5bd.

openFDA Drug LabelsOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Drug label update: Colgate Max Fresh Cool Mint

Official structured record identifier: 00652bb2-090c-4eaa-8fc2-e0be6913a724.

openFDA Drug LabelsOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Drug recall: CHLORAPREP ONE-STEP

Official structured record identifier: 99377.

openFDA Drug RecallsOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Drug recall: CLEVIPREX

Official structured record identifier: 99376.

openFDA Drug RecallsOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Drug recall: NYSTATIN

Official structured record identifier: 99283.

openFDA Drug RecallsOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Drug recall: QUALITY CHOICE EARWAX REMOVAL KIT

Official structured record identifier: 99278.

openFDA Drug RecallsOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Device recall: Rapid Refill Continuous Injection System, UPN M00566001

Official structured record identifier: 99336.

openFDA Device RecallsOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Device recall: Photera 600 3-D, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders

Official structured record identifier: 99331.

openFDA Device RecallsOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Device recall: Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK DYNJT6267

Official structured record identifier: 99318.

openFDA Device RecallsOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Device recall: Optima XR200amx, Mobile Digital-Ready Radiographic System

Official structured record identifier: 99279.

openFDA Device RecallsOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Device recall: The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000; UDI 00607567700406) is a sterile, single-use Class II device that was cleared for marketing by FDA under 510(k) number K101274.

Official structured record identifier: 99259.

openFDA Device RecallsOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Device recall: Orthofix MINIRAIL, STANDARD LENGTHENER Model/Catalog Number: M101, Unilateral orthopedic/trauma external fixation device

Official structured record identifier: 99225.

openFDA Device RecallsOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Device recall: ST AIA-Pack Testosterone, IN VITRO DIAGNOSTIC USE ONLY for the quantitative measurement of testosterone in human serum on specific Tosoh AIA System analyzers, Model Number 0025204

Official structured record identifier: 99210.

openFDA Device RecallsOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Device recall: Medtronic Bio-Medicus Adult Cannula Kit, Product Number/CFN 96530-115; Cardiopulmonary bypass vascular cannula

Official structured record identifier: 99199.

openFDA Device RecallsOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Device recall: ICU Medical Plum Duo Infusion Pump, v1.2.3: 1) Item Number 400020401 and 2) Item Number 400020403; infusion pump

Official structured record identifier: 99192.

openFDA Device RecallsOriginal source
馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source

Device recall: Abiomed REF: 0052-3025, Introducer Kit for Impella Hemostatic Peel Away Introducer System with Infusion Sideport, 14F 13cm and 25cm. heart pump and accessories.

Official structured record identifier: 99102.

openFDA Device RecallsOriginal source