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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🌍discoverynews.google.comTier 3 · Aggregated media

Kelun-Biotech’s sac-TMT Plus Pembrolizumab Hits Primary Endpoint in PD-L1-Negative NSCLC

The Clinical Trial VanguardOriginal source
🇺🇰Devicespresspart.comTier 1 · Company source

Medical Technology Ireland 2026

H&T PresspartOriginal source
🌍discoverynews.google.comTier 3 · Aggregated media

Claiming 9.77 billion yuan! Cathay Biotech launches large-scale trade secret litigation

ChemNetOriginal source
🌍Industryamarin.co.thTier 3 · Secondary coverage

บ้านและสวนแฟร์ Midyear 2026

Amarin CorporationOriginal source
🌍discoverynews.google.comTier 3 · Aggregated media

REG - RTW Biotech Opp. - Monthly Valuation Update and Factsheet

TradingViewOriginal source
🌍discoverynews.google.comTier 3 · Aggregated media

Enterprise value to EBITDA forward of Maxigen Biotech Inc. – TWSE:1783

TradingViewOriginal source
🇯🇵Industrysumitomo-pharma.comTier 1 · Company source

Development of the Regenerative Medicine Product “AMCHEPRY” Receives the 10th Japan Bioindustry Award

Sumitomo PharmaOriginal source
🌍discoverynews.google.comTier 3 · Aggregated media

Sudan’s embassy in India hosts roundtable on investment opportunities in pharmaceutical and healthcare sectors

MSNOriginal source
🌍discoverynews.google.comTier 2 · Trade media

Biotech IPOs surge in H1 of 2026, shattering records and doubling last year’s total

BioSpaceOriginal source
🌍discoverynews.google.comTier 3 · Aggregated media

Why is Tasly Pharmaceutical stock rallying today?

Investing.comOriginal source
🌍discoverynews.google.comTier 3 · Aggregated media

Pharmaceutical marketplaces: How online platforms are changing drug purchasing

KRDOOriginal source
🌍discoverynews.google.comTier 3 · Aggregated media

Israel-based ocular disease biotech Tarsier Pharma ups shares offered by 11% ahead of $50 million US IPO

renaissancecapital.comOriginal source
🌍discoverynews.google.comTier 3 · Aggregated media

BRVE IPO News - Cardiovascular diseases biotech Braveheart Bio files for a $100 million IPO

renaissancecapital.comOriginal source
🇺🇸Regulatoryfda.govTier 1 · Regulatory source

Early Alert: Ventilator Issue from Resmed

Failure of an electrical component in certain Astral ventilators may cause an interruption or failur...

FDA MedWatchOriginal source
🌍discoverynews.google.comTier 3 · Aggregated media

Enterprise value to EBIT forward of Jin Yang Pharmaceutical Co., Ltd. – KRX:007370

TradingViewOriginal source
🌍discoverynews.google.comTier 3 · Aggregated media

Celltrion Begins Phase 1 Trial in South Korea for Biosimilar of $5.2 Billion Blockbuster Tremfya

finance.biggo.comOriginal source
🇩🇪Mediacharite.deTier 2 · Direct publisher

Überzogene Forderungen bei Tarifverhandlungen gehen zu Lasten von Patienten und Mitarbeitenden

Charité - Universitätsmedizin Berlin (EN)Original source
🌍discoverynews.google.comTier 3 · Aggregated media

Price to earnings forward of Jin Yang Pharmaceutical Co., Ltd. – KRX:007370

TradingViewOriginal source
🌍discoverynews.google.comTier 3 · Aggregated media

Spain signals new direction on EU biotech innovation

euractiv.comOriginal source
🌍discoverynews.google.comTier 3 · Aggregated media

Maha FDA cracks down on blood centres, suspends 34 licences and cancels 4 for violating drug norms

Pharmabiz.comOriginal source
🌍discoverynews.google.comTier 3 · Aggregated media

Study supports Onconic's Jaqbo co-use with common cardiovascular drugs

koreabiomed.comOriginal source
🌍discoverynews.google.comTier 2 · Trade media

Biotech Visionary John F. Crowley to Keynote Emily Whitehead Foundation's 2026 Believe Ball in Philadelphia

BioSpaceOriginal source
🌍discoverynews.google.comTier 3 · Aggregated media

Celltrion Ends European Keytruda Biosimilar Trial

BusinesskoreaOriginal source
🌍discoverynews.google.comTier 3 · Aggregated media

West Pharmaceutical Services (WST) Enters Strategic Agreements w

GuruFocusOriginal source
🌍discoverynews.google.comTier 3 · Aggregated media

FDA lets Leqembi start at home with 15-second subcutaneous shots - CHOSUNBIZ

ChosunbizOriginal source
🌍discoverynews.google.comTier 3 · Aggregated media

Is Krystal Biotech (KRYS) Too Expensive After A 440% Return?

simplywall.stOriginal source
🌍discoverynews.google.comTier 3 · Aggregated media

FDA Clears Atrium Therapeutics' IND Application for Cardiomyopathy Drug

dicardiology.comOriginal source
🌍discoverynews.google.comTier 3 · Aggregated media

Teva Pharmaceutical Industries (TEVA) Advances TEV 408, Is The Stock Still Cheap?

simplywall.stOriginal source
🇺🇸Regulatorysec.govTier 1 · Regulatory source

Johnson & Johnson filed Form 8-K

SEC EDGAROriginal source
🇺🇸Regulatorysec.govTier 1 · Regulatory source

GSK filed Form 6-K

SEC EDGAROriginal source
🇺🇰Regulatorynice.org.ukTier 1 · Regulatory source

View all in-depth

NICEOriginal source
🇸🇬Regulatoryhsa.gov.sgTier 1 · Regulatory source

30 June 2026Regulatory Update for Therapeutic Product Registration (30 June 2026)AudiencesIndustry memberProduct typeTherapeutic ProductsExtension of e-labelling to P and GSL medicinesRegulatory Updates

Extension of e-labelling to P and GSL medicines

HSA (Singapore)Original source
🇺🇸Regulatoryfederalregister.govTier 1 · Regulatory source

National Institute on Minority Health and Health Disparities; Notice of Partially Closed Meeting

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

Center For Scientific Review; Notice of Closed Meetings

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

Submission for Office of Management and Budget Review; Office of Refugee Resettlement Unaccompanied Refugee Minors Program Application and Withdrawal of Unaccompanied Refugee Minors Program Application or Declination of Unaccompanied Refugee Minors Program Placement Forms

The Office of Refugee Resettlement is requesting a 3-year extension with revisions of the Unaccompan...

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

Meetings of the Presidential Advisory Council on Combating Antibiotic-Resistant Bacteria

As stipulated by the Federal Advisory Committee Act, the Department of Health and Human Services (HH...

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

Request for Information (RFI): Inviting Comments and Suggestions on Topic Areas for the NIDCR Strategic Plan for Fiscal Years 2027-2031

The National Institute of Dental and Craniofacial Research (NIDCR) is developing its Strategic Plan...

Federal RegisterOriginal source
🇹🇭Regulatoryfda.moph.go.thTier 1 · Regulatory source

15 ก.ค. 69ข่าวประกาศผลการตรวจพิสูจน์อาหาร อย. แจ้งเตือนประชาชน หยุดบริโภคผลิตภัณฑ์อาหาร 25 รายการ หลังตรวจพบเป็นอาหารปลอมอ่านเพิ่มเติม →

สำนักงานคณะกรรมการอาหารและยา ได้ประสานสำนักงานสาธารณสุขจังหวัดศรีสะเกษ ดำเนินการตรวจสอบสถานที่ผลิตอา...

Thai FDAOriginal source
🇹🇭Regulatoryfda.moph.go.thTier 1 · Regulatory source

15 ก.ค. 69อย. เตือน ผลิตภัณฑ์เสริมอาหาร “วิสโตริน” อ้างรักษาโรคทางตาอ่านเพิ่มเติม →

สำนักงานคณะกรรมการอาหารและยา (อย.) ได้รับเรื่องร้องเรียนให้ตรวจสอบผลิตภัณฑ์เสริมอาหาร “วิสโตริน” ขาย...

Thai FDAOriginal source
🇩🇪Industrybayer.comTier 1 · Company source

Bayer signs licensing agreement with RAGT and begins broad hybrid wheat commercialization by early 2030s

Licensing agreement enables Bayer to scale franchise in Europe and North America simultaneously / Ba...

Bayer PharmaceuticalsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source

Drug label update: Acetaminophen Extra Strength

Official structured record identifier: 9d34abc2-3a9a-b68f-80d4-4ede1eb1e45f.

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

Drug label update: Allergy Relief

Official structured record identifier: 44da36d2-1881-e779-d3a2-13ea828f9240.

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

Drug label update: Acetaminophen

Official structured record identifier: 3f182571-3212-eb29-e063-6294a90a9fa0.

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

Drug recall: Pemetrexed for Injection 500mg/Vial, 1 50 mL Single-Dose Vial per carton, For intravenous use only, Rx only, Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873 NDC: 70069-0835-01

Official structured record identifier: 99312.

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

Drug recall: Methohexital Sodium, 100 mg/10 mL (10 mg/mL), Total Volume: 10 mL, Rx only, Compounded drug, QuVa Pharma, 1075 W Park One Dr, Suite 100, Sugar Land, TX 77478, Product code: 70092-1310-46.

Official structured record identifier: 99311.

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

Drug recall: MEDLINE

Official structured record identifier: 99234.

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

Drug recall: Clomiphene Citrate USP Active Pharmaceutical Ingredient (CAS : 50-41-9), Net Weight a)1 KG (NDC 84849-000-01), b) 500 g (NDC 84849-000-02), (c) 100 g (NDC 84849-000-03), Rx Only, Shimoga Chemicals Address -W-57A, MIDC Kupwad Samgli, Maharashtra, 416436, India.

Official structured record identifier: 99232.

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

Drug recall: METHOHEXITAL SODIUM

Official structured record identifier: 99220.

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

Drug recall: Gasco Isopropyl Alcohol 70%, Net Contents: 1 US Gallon (3.78 L), Manufactured by: Gasco Industrial Corp., PO Box 1360, Gurabo, PR 00778, Made in USA

Official structured record identifier: 99138.

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

Device recall: Brand Name: Versius Surgical System US Product Name: Vesius Surgeon Console US Model/Catalog Number: V-SS-1020 Software Version: Pratchett 1 version 62.1 Product Description: The Versius Surgical System is a modular, open console, software controlled, electromechanical system designed

Official structured record identifier: 99280.

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

Device recall: KL Owen Custom Orthodontic Solution, model/catalog number CIAS-800033,

Official structured record identifier: 99277.

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

Device recall: TMINI Femur Tracking Array REF 109003 UDI-DI code: M9461090030 TMINI Tibia Tracking Array REF 109004 UDI-DI code: M9461090040 TMINI Miniature Robotic System is indicated as a stereotaxic instrumentation system for total knee replacement (TKA) surgery. It is to assist the surgeon by pr

Official structured record identifier: 99219.

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

Device recall: Atellica CH Enzymatic Hemoglobin A1c (A1c_E). Material Number: 11097536.

Official structured record identifier: 99214.

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

Device recall: VITEK 2 AST-N447 TEST KIT Product reference 424620

Official structured record identifier: 99213.

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

Device recall: MiniMed 780G Insulin Pump, REF: MMT-1885, MMT-1886, MMT-1895, MMT-1896

Official structured record identifier: 99207.

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

Device recall: Medline Convenience Kits: 1) ANESTHESIA KIT PEDS 90-LF, Model Number: DYNJAP10125A

Official structured record identifier: 99196.

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

Device recall: OmniTract Surgical Retractor System, which includes 633 of the firm s product codes.

Official structured record identifier: 99193.

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

Device recall: Aquacel Ag Surgical SP REF: 413556 9cm x 15cm/3.5 in. x 6 in., Sterile R

Official structured record identifier: 99151.

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

Device recall: Olympus Single Use Distal Cover, Catalog Number MAJ-2315, Used with: EVIS EXERA III Duodenovideoscope TJF-Q190V- designed to be attached to Olympus duodenovideoscopes to cover the distal end of the insertion tube and around the forceps elevator; duodenoscope and accessories, flexible/

Official structured record identifier: 99106.

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

Device recall: GSP Neonatal GALT Kit. Product Codes: 3303-001U, 3303-0010. in vitro diagnostic. Used in FLUORESCENT PROC. (QUAL), GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE.

Official structured record identifier: 99065.

openFDA Device RecallsOriginal source