PharmaRadar360
PharmaRadar360
Intelligence Layer

Pharma intelligence feed

Latest pharma feed

426
Indexed signals
Latest
Coverage mode
All sectors
Active lens

News stream

Latest stories

Showing 140 of 426 stories

Track keywords
🇮🇪Devicesiconplc.com

Industry events

ICON plc· Original source
🌍Industryinvestor.lilly.com

Phase 3b data presented at AAD Annual Meeting show Lilly's Taltz (ixekizumab) plus Zepbound (tirzepatide) delivered superior efficacy for adults with psoriatic arthritis and obesity

Eli Lilly· Original source
🇺🇸Industryjnj.com

ICOTYDE™ (icotrokinra) one-year results confirm lasting skin clearance and favorable safety profile in once‑daily pill for plaque psoriasis

Johnson & Johnson presents new data showing high rates of complete skin clearance achieved at Week 2...

Johnson & Johnson News· Original source
🇺🇸Industrynews.bms.com

Open Label Outpatient Switch Study Demonstrates Symptom Stability During Transition from Oral Atypical Antipsychotics to Cobenfy™ (xanomeline and trospium chloride)

Bristol Myers Squibb (Global)· Original source
🇺🇸Industryamgen.com

REPATHA® CUTS RISK OF FIRST MAJOR CARDIOVASCULAR EVENTS BY 31% IN HIGH-RISK PATIENTS WITHOUT KNOWN SIGNIFICANT ATHEROSCLEROSIS

Repatha is the Only PCSK9 Inhibitor to Significantly Reduce the Risk of First CV Events in High-Risk...

Amgen (Global News)· Original source
🌍Industryinflarx.de

Cantor Global Healthcare Conference 2025

InflaRx· Original source
🌍Industryinflarx.de

2025 Jefferies Global Healthcare Conference

InflaRx· Original source
🌍Industryinflarx.de

Leerink Global Healthcare Conference

InflaRx· Original source
🇺🇸Regulatoryfda.gov

Generic Drug User Fee Amendments

This page features news and information for industry and stakeholders about GDUFA, its fee structure...

FDA Drug Approvals· Original source
🇺🇸Regulatoryfda.gov

What’s New for Biologics

Latest news from the Center for Biologics Evaluation and Research

FDA CBER (Biologics)· Original source
🇺🇸Regulatoryfda.gov

Switching Between Biosimilars and Their Reference Counterparts with Dr. Sarah Yim

Listen to our latest podcast series, Q&A with FDA, on Switching Between Biosimilars and Their Refere...

FDA Drug Approvals· Original source
🇬🇧Regulatorygov.uk

Decision: Medical devices given exceptional use authorisations

List of manufacturers and their medical devices granted an exemption by MHRA. The list also includes...

MHRA UK· Original source
🇺🇸Regulatoryfda.gov

What's New Related to Drugs

Want to know what's new on drugs from FDA? This page provides quick links to the latest on a variety...

FDA Drug Approvals· Original source
🇬🇧Regulatorygov.uk

Clinical trials for medicines: guidance on quality and risk proportionality

Information on applying quality by design, risk‑based quality management, and proportionate oversigh...

MHRA UK· Original source
🇬🇧Regulatorygov.uk

Clinical trials for medicines: guidance on compliance with ICH E6 good clinical practice (GCP) in the United Kingdom

Information on how ICH E6(R3) good clinical practice (GCP) principles are implemented and enforced i...

MHRA UK· Original source
🇺🇸Industrynews.abbvie.com

AbbVie to Highlight New Clinical and Real-World Evidence Advancing Standards of Care in Immune-Mediated Skin Diseases at the 2026 AAD Annual Meeting

Data highlights efficacy and safety of risankizumab in psoriatic disease, including high impact area...

AbbVie News· Original source
🇺🇸Regulatoryfda.gov

Resource Capacity Planning and Modernized Time Reporting

FDA is making optimal use of its financial resources to maximize its ability to efficiently and effe...

FDA Drug Approvals· Original source
🌍Industryinvestor.lilly.com

Lilly's EBGLYSS (lebrikizumab-lbkz) delivered up to four years of durable disease control for patients with moderate-to-severe atopic dermatitis

Eli Lilly· Original source
🇬🇧Researchroyalmarsden.nhs.uk

Screening Programme detects thousands of lung cancers early with potential to save lives

The programme uses low-dose computed tomography (LDCT) scans to identify lung cancer at an earlier,...

The Royal Marsden NHS Foundation Trust· Original source
🇬🇧Industrygsk.com

27 March 2026Bepirovirsen accepted for review by the European Medicines Agency as a potential first-in-class treatment for chronic hepatitis BSubmission supported by statistically significant and clinically meaningful functional cure rates in pivotal PhIII B-Well trials

GSK RSS· Original source
🌍Researchscience.org

‘Milestone’ research method measures gene activity across whole mice

Science· Original source
🇬🇧Researchpubmed.ncbi.nlm.nih.gov

Bullous haemorrhagic cellulitis caused by Escherichia coli in a patient with cirrhosis

PubMed Lancet Infectious Diseases RSS· Original source
🇬🇧Researchpubmed.ncbi.nlm.nih.gov

Double-dose azithromycin mass drug administration, facial cleanliness, and fly control measures for trachoma control in Oromia, Ethiopia (Stronger SAFE): a cluster-randomised controlled trial

PubMed Lancet Infectious Diseases RSS· Original source
🇺🇸Researchpubmed.ncbi.nlm.nih.gov

Ethical Design and Implementation of Monetary Transfer Interventions in Clinical Cancer Research

PubMed Journal of Clinical Oncology RSS· Original source
🇺🇸Researchpubmed.ncbi.nlm.nih.gov

Radiographic Progression With and Without Prostate-Specific Antigen Rise in Patients With Advanced Prostate Cancer Treated With Enzalutamide

PubMed Journal of Clinical Oncology RSS· Original source
🇺🇸Researchpubmed.ncbi.nlm.nih.gov

Phase I Study of Mosperafenib, a Novel Paradox Breaker B-Raf Proto-Oncogene Serine/Threonine Kinase (BRAF) Inhibitor, in Patients With BRAF V600-Mutant Solid Tumors

PubMed Journal of Clinical Oncology RSS· Original source
🇺🇸Researchpubmed.ncbi.nlm.nih.gov

Molecular-Based Ecosystem to Improve Personalized Medicine in Chronic Myelomonocytic Leukemia

PubMed Journal of Clinical Oncology RSS· Original source
🇺🇸Researchpubmed.ncbi.nlm.nih.gov

IGH::FENDRR and specific KRAS mutations define a novel B-ALL molecular subtype with poor chemotherapy response

PubMed Blood RSS· Original source
🇨🇭Industrynovartis.com

Press releaseMar 27, 2026Novartis agrees to acquire Excellergy, Inc., building on allergy leadership with next-generation anti-IgE innovation- Proposed acquisition strengthens Novartis immunology strategy in food allergy and other IgE-driven diseases - Lead asset Exl-111 builds on proven IgE biology with a differentiated…

- Proposed acquisition strengthens Novartis immunology strategy in food allergy and other IgE-driven...

Novartis News· Original source
🇸🇪Industrysobi.com

Notice of Annual General Meeting in Swedish Orphan Biovitrum AB (publ)

The shareholders in Swedish Orphan Biovitrum AB (publ) (Sobi®) Reg. No. 556038-9321, are hereby summ...

Swedish Orphan Biovitrum· Original source
🇯🇵Regulatorypmda.go.jp

[ANZEN]PMDA Risk Communications: Infliximab (genetical recombination) etc. posted

医薬品・医療機器・再生医療等製品の承認審査・安全対策・健康被害救済の3つの業務を行う組織。

PMDA Japan· Original source
🇯🇵Regulatorypmda.go.jp

[SHINSA]Document-based Inspection to CTD M3(Quality studies)/M4(Non-clinical studies other than GLP studies) data page created

医薬品・医療機器・再生医療等製品の承認審査・安全対策・健康被害救済の3つの業務を行う組織。

PMDA Japan· Original source
🌍Researchscience.org

These small African antelopes may help mpox spread

Science· Original source
🌍Regulatorypharmac.govt.nz

Agenda for April 2026 Cancer Treatments advisory committee (CTAC) meeting

Information on what the Cancer Treatments Advisory Committee (CTAC) will be considering at its upcom...

Pharmac New Zealand· Original source
🌍Regulatoryema.europa.eu

New treatment for relapsed extensive-stage small cell lung cancer

Imdylltra addresses unmet need in people with poor prognosis and limited treatment options

EMA Human Medicines· Original source
🌍Regulatoryema.europa.eu

Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 23-26 March 2026

Five new medicines recommended for approval; another 13 medicines recommended for extension of their...

EMA Human Medicines· Original source
🌍Regulatoryema.europa.eu

EMA recommends restricting use of Tecovirimat SIGA

The medicine was not effective for the treatment of mpox in randomised clinical trials

EMA Human Medicines· Original source
🇬🇧Researchnature.com

AI-driven body composition atlas reveals its association with NSCLC immunotherapy outcome and molecular background: a multicenter study

npj Precision Oncology· Original source
🇬🇧Researchnature.com

Risk assessment of secondary primary malignancies: results from two large prospective European cohorts

npj Precision Oncology· Original source
🇬🇧Researchnature.com

A comprehensive foundation model for generalizable cytogenetics in precision oncology with CHROMA

npj Precision Oncology· Original source
🇬🇧Industryastrazeneca.com

Tozorakimab met primary endpoint in both OBERON and TITANIA Phase III trials in patients with COPD

Positive high-level results from the Phase III OBERON and TITANIA trials in patients with chronic ob...

AstraZeneca News· Original source
🇫🇷Industrysanofi.com

2026 03 27 12 00 00 3263711

Sanofi’s Sarclisa subcutaneous formulation administered via on-body injector recommended for EU appr...

Sanofi News· Original source
🇯🇵Industryshionogi.com

Notice Regarding Bridge Loan Financing in Connection with an Additional Investment in ViiV Healthcare Ltd

Shionogi (IR News)· Original source
🇺🇸Researchcedars-sinai.org

Spectrum News 1: Cedars-Sinai Researchers Create New AI-Based System to Read Echocardiograms

Cedars-Sinai cardiologist David Ouyang told Spectrum News 1 about a new AI tool that can read echoca...

Cedars-Sinai Medical Center· Original source
🌍Regulatoryispe.org

Bioprocess Online Covers Novo Nordisk Feature at the 2026 ISPE Facilities of the Future Conference

During a sustainability panel at the 2026 ISPE Facilities of the Future Conference, Larry Lane and J...

ISPE (International Society for Pharmaceutical Engineering)· Original source
🇺🇸Industrybiomarin.com

An Open Letter to the Pompe and Fabry Communities

Learn more about BioMarin's origin story and longstanding commitment to rare diseases in this open l...

BioMarin Pharmaceutical· Original source
🇺🇸Industrygsk.com

View latest results

Stiefel (GSK)· Original source
🌍Regulatoryfda.gov.tw

公告115年度「國家藥物科技研究發展獎」自公告日起至115年6月30日止受理申請。

公告115年度「國家藥物科技研究發展獎」自公告日起至115年6月30日止受理申請。

TFDA Taiwan· Original source
🌍Industryorionpharma.com

Medicine deliveries continue despite the conflict in the Middle East3/27/2026 Orion Pharma and Society

Global supply chains have remained resilient despite the escalating conflict in the Middle East. Whi...

Orion Corporation· Original source
🇺🇸Industryir.ideayabio.com

IDEAYA Biosciences Announces Inducement Grants under Nasdaq Listing Rule 5635(c)(4)

IDEAYA Biosciences, Inc. (NASDAQ: IDYA), a precision medicine oncology company committed to the disc...

IDEAYA Biosciences· Original source
🇯🇵Industryotsuka.co.jp

27 MAR 2026PharmaceuticalsOtsuka Pharmaceutical to Acquire Transcend Therapeutics - Expands Otsuka portfolio in psychiatric and neurological fields and aims to accelerate development of Transcend’s portfolio, including the TSND-201 program for post-traumatic stress disorder (PTSD)

Otsuka Pharmaceutical Co., Ltd News Releases

Otsuka Pharmaceutical· Original source
🇯🇵Industryotsuka.co.jp

27 MAR 2026PharmaceuticalsOtsuka Submits Application in Japan for Iclusig®for First-Line Treatment of Philadelphia Chromosome-Positive Acute Lymphoblastic Leukemia

Otsuka Pharmaceutical Co., Ltd News Releases

Otsuka Pharmaceutical· Original source
🇮🇳Regulatorypib.gov.in

PharmaMed 2026 का समापन

Press Information Bureau (PIB) is the nodal agency of the Government of India to disseminate informa...

PIB India Healthcare· Original source
🇺🇸Industryzoetis.com

Feature Stories

Zoetis is a global animal health company dedicated to supporting customers and their businesses in e...

Zoetis· Original source
🇩🇪Regulatoryvfa.de

27.03.2026 [PM 007/26]Mehr Frauenerwerbstätigkeit stärkt Arbeitsmarkt und WachstumDeutschland ist so fleißig wie nieMehr Frauenerwerbstätigkeit stärkt FachkräftebasisTeilzeit, weibliche Führungskräfte und Vergütung sind...

Mehr Frauenerwerbstätigkeit stärkt Arbeitsmarkt und Wachstum Mehr Frauenerwerbstätigkeit stärkt Fach...

VFA Germany· Original source
🇩🇰Industrybavarian-nordic.com

Bavarian Nordic Submits Data to EMA to Extend Mpox and Smallpox Vaccine Approval to Children Aged 2-11 Years

Bavarian Nordic· Original source
🇮🇪Industryir.prothena.com

Irish Statutory Financial Statements

Investors - Financials & Filings - Irish Statutory Financial Statements | Prothena Corporation plc

Prothena· Original source
🌍Industrygedeonrichter.com

20260327 Whc Reg

Gedeon Richter Investors Announcements Richter receives European Commission approval for FYLREVY® (E...

Gedeon Richter· Original source
🇺🇸Regulatoryfda.gov

FDA Approves First Gene Therapy for Severe Leukocyte Adhesion Deficiency Type I

The U.S. Food and Drug Administration today approved Kresladi (marnetegragene autotemcel), the first...

FDA News· Original source
🇺🇸Regulatoryfda.gov

Over-The-Counter Monograph Drug User Fee Program (OMUFA)

A user fee program for nonprescription (over-the-counter or OTC) monograph drugs would be a potentia...

FDA Drug Approvals· Original source
🇬🇧Regulatorygov.uk

Guidance: Archiving and retention of clinical trial records

Information on clinical trial record retention and archiving requirements including requirements for...

MHRA UK· Original source
🇬🇧Regulatorygov.uk

Clinical trials for medicines: good manufacturing practice and radiopharmaceutical investigational medicinal products

Guidance on good manufacturing practice and the use of radiopharmaceutical investigational medicinal...

MHRA UK· Original source
🌍Regulatoryravimiamet.ee

Accelerated assessment procedures support the conduct of drug trials in Estonia and Europe

The State Agency of Medicines has established a national accelerated assessment procedure and is als...

SAM Estonia· Original source
🇬🇧Regulatorygov.uk

Transparency data: MHRA Performance Data

Performance data for MHRA key performance indicators (KPIs) and information on the expected timeline...

MHRA UK· Original source
🇺🇸Researchpubmed.ncbi.nlm.nih.gov

Sevabertinib in Advanced HER2-Mutant Non-Small-Cell Lung Cancer. Reply

PubMed NEJM RSS· Original source
🇺🇸Researchpubmed.ncbi.nlm.nih.gov

Sacituzumab Govitecan in Advanced Triple-Negative Breast Cancer. Reply

PubMed NEJM RSS· Original source
🇺🇸Researchpubmed.ncbi.nlm.nih.gov

Phase 1 Trial of CRISPR-Cas9 Gene Editing Targeting ANGPTL3. Reply

PubMed NEJM RSS· Original source
🇺🇸Researchpubmed.ncbi.nlm.nih.gov

Phase 1 Trial of CRISPR-Cas9 Gene Editing Targeting ANGPTL3

PubMed NEJM RSS· Original source
🇬🇧Researchpubmed.ncbi.nlm.nih.gov

New WHO recommendations for tuberculosis diagnosis

PubMed Lancet Infectious Diseases RSS· Original source
🇬🇧Researchpubmed.ncbi.nlm.nih.gov

Methodological quality assessment tool for observational studies comparing treatment effectiveness in infectious diseases: a Delphi consensus and application to studies on bloodstream infections due to carbapenem-resistant Enterobacterales

PubMed Lancet Infectious Diseases RSS· Original source
🇺🇸Researchpubmed.ncbi.nlm.nih.gov

Final Efficacy and Safety Data From the Phase I/II ARROW Study of Pralsetinib in Patients With Advanced RET Fusion-Positive Non-Small Cell Lung Cancer

PubMed Journal of Clinical Oncology RSS· Original source
🇺🇸Researchpubmed.ncbi.nlm.nih.gov

Old Dog, New Tricks: Oxybutynin for the Treatment of Androgen Deprivation Therapy-Related Vasomotor Symptoms

PubMed Journal of Clinical Oncology RSS· Original source
🇺🇸Researchpubmed.ncbi.nlm.nih.gov

Targeting enhancer RNAs to silence transcription

PubMed Blood RSS· Original source
🇺🇸Researchpubmed.ncbi.nlm.nih.gov

Benchmarking clonal hematopoiesis in sickle cell disease

PubMed Blood RSS· Original source
🇺🇸Researchpubmed.ncbi.nlm.nih.gov

Mandato E, Yan Q, Ouyang J, et al. MYD88L265P augments proximal B-cell receptor signaling in large B-cell lymphomas via an Interaction with DOCK8. Blood. 2023;142(14):1219-1232

PubMed Blood RSS· Original source
🇩🇰Industrylundbeckfonden.com

The Lundbeck Foundation Annual Report 2025

In 2025, the Lundbeck Foundation delivered strong financial results and maintained a high level of g...

Lundbeckfonden (News)· Original source
🇪🇸Regulatoryaemps.gob.es

OMNIPAQUE 300 mg, OMNIPAQUE 350 mg Iodo /ml SOLUCION INYECTABLE y VISIPAQUE 320 mg /ml SOLUCION INYECTABLE

Formato pdf Fecha de publicación: 26 de marzo de 2026 Nº alerta: R_16/2026 Fecha: 25 de marzo de 202...

AEMPS (Spain)· Original source
🇪🇸Regulatoryaemps.gob.es

La AEMPS informa de la detección de un lote falsificado de cánulas nasales con conexión luer-lock para adultos

Generar PDF Fecha de publicación: 26 de marzo de 2026 Categoría: productos sanitarios, productos fal...

AEMPS (Spain)· Original source
🇧🇪Industryglpg.com

Galapagos Announces Nomination of Gino Santini to its Board of Directors

Galapagos (News)· Original source
🇧🇪Industryglpg.com

Galapagos Publishes 2025 Annual Report and Announces Annual and Extraordinary Shareholders’ Meetings

Galapagos (News)· Original source
🇺🇸Industrynews.abbvie.com

Allergan Aesthetics Reinforces Scientific Differentiation and Leadership with 21 Evidence-Based E-Posters at the 2026 Aesthetic & Anti-Aging Medicine World Congress (AMWC)

- Five scientific e-posters highlight investigational neurotoxin trenibotulinumtoxinE (TrenibotE), d...

AbbVie News· Original source
🇺🇸Industrynews.abbvie.com

Allergan Aesthetics Ushers in a New Age of Hyaluronic Acid (HA) Injectables with JUVÉDERM® at AMWC Monaco

Research reveals an industry mindset shift towards 'undetectable†' aesthetics, as people seek a natu...

AbbVie News· Original source
🇫🇷Industryinnate-pharma.com

Innate Pharma reports full year 2025 financial results and business update

Lacutamab TELLOMAK-3 confirmatory Phase 3 trial in cutaneous T-cell lymphoma (CTCL) is planned for i...

Innate Pharma (IR)· Original source
🌍Regulatorybasg.gv.at

„Medikamente Info Austria“ liefert kompakte Medikamenten-Information im neuen Design

Mit 10. Februar 2026 beginnt der Echtbetrieb für das neue Medikamenten-Informationssystem des Bundes...

BASG Austria· Original source
🌍Regulatorywho.int

World report on promoting the health of refugees and migrants: Monitoring progress on the WHO global...

The report calls for stronger leadership, sustained investment and enhanced coordination to promote...

WHO (Pharma/Health Innovation)· Original source
🇩🇰Industrynovonordisk.com

Investor Highlights.Html

Here you will get an overview of all the information and services that we provide for you as a Novo...

Novo Nordisk News· Original source
🇨🇦Industryir.bauschhealth.com

Bausch Health Announces Ortho Dermatologics 2026 ASPIRE HIGHER Scholarship Program

Bausch Health (IR News)· Original source
🇯🇵Industrytakeda.com

Financial Highlights

Takeda provides annual and quarterly financial highlights, statements, and data for investors. Data...

Takeda News· Original source
🌍Regulatoryefpia.eu

Statements & press releases26.03.26PFAS restrictions: risks for patients and companies operating in EuropeRead Article

EFPIA reaction to the publication of ECHA scientific committees’ opinions on PFAS Restriction. The p...

EFPIA Europe· Original source
🇺🇸Industryfinnegan.com

Finnegan Receives Gold Level Healthy Workforce Designation and Bicycle Friendly Business Award

Finnegan IP (Life Sciences focus)· Original source
🇩🇪Regulatoryvfa.de

26.03.2026 [PM 006/26]Daten als Standortfaktor: EHDS stärkt Europas Forschung und InnovationEHDS schafft größten vernetzten Datenraum für Gesundheitsdaten weltweitMehr Dynamik in klinischer Forschung und InnovationNationale Umsetzung...

Daten als Standortfaktor: EHDS stärkt Europas Forschung und Innovation EHDS schafft größten vernetzt...

VFA Germany· Original source
🌍Industryjulphar.net

Financial Reports - 2025

Financial Reports Financial Reports - 2026 Financial Reports - 2025 Financial Reports - 2024 Financi...

Julphar Gulf Pharma· Original source
🇯🇵Industryono-pharma.com

Mar.26.2026R & DOno Pharma Submits an Application for Approval of Ripretinib (DCC-2618) in Patients with Advanced Gastrointestinal Stromal Tumor in Japan

Application submitted for manufacturing and marketing approval of ripretinib in Japan for the indica...

Ono Pharmaceutical· Original source
🌍Regulatoryhta.callaghaninnovation.govt.nz

Mar 26, 2026Internal3HTA Monthly Wrap - March 2026The latest in NZ healthtech, including upcoming events, sector news and insightsRead more

The latest in NZ healthtech, including upcoming events, sector news and insights

HealthTech NZ· Original source
🇪🇸Industryalmirall.com

AAD 2026: Almirall presents new clinical and real‑world evidence across atopic dermatitis, psoriasis, actinic keratosis and acne

Almirall advances scientific leadership in medical dermatology with new data across atopic dermatiti...

Almirall· Original source
🇺🇸Regulatoryfda.gov

Regulatory Education for Industry (REdI) Annual Conference 2026: Innovative Regulatory Strategies to Advance Medical Products - 05/19/2026

Learn directly from the FDA’s regulatory experts in medical product centers: drugs, devices, and bio...

FDA CBER (Biologics)· Original source
🇬🇧Regulatorygov.uk

Guidance: Medicines that you cannot export from the UK or hoard

Sets out medicines that cannot be exported from the UK or hoarded because they are needed for UK pat...

MHRA UK· Original source
🇺🇸Regulatoryfda.gov

Workshops, Meetings & Conferences (Biologics)

Information on CBER sponsored or co-sponsored meetings, conferences and workshops about various biol...

FDA CBER (Biologics)· Original source
🇬🇧Regulatorygov.uk

Shaping the Future of Healthcare Through Global Regulatory Innovation

Emerging technologies like AI and advanced therapies are transforming healthcare, and through intern...

MHRA UK· Original source
🇺🇸Regulatoryfda.gov

FDA Approves Drug to Treat Neurologic Manifestations of Hunter Syndrome

The U.S. Food and Drug Administration approved Avlayah (tividenofusp alfa-eknm) to treat certain ind...

FDA News· Original source
🇬🇧Industryastrazeneca.com

Tozorakimab met primary endpoint in both OBERON and TITANIA Phase III trials in patients with COPD

Positive high-level results from the Phase III OBERON and TITANIA trials in patients with chronic ob...

AstraZeneca News· Original source
🇫🇷Industrysanofi.com

2026 03 27 12 00 00 3263711

Sanofi’s Sarclisa subcutaneous formulation administered via on-body injector recommended for EU appr...

Sanofi News· Original source
🇯🇵Industryshionogi.com

Notice Regarding Bridge Loan Financing in Connection with an Additional Investment in ViiV Healthcare Ltd

Shionogi (IR News)· Original source
🇺🇸Researchcedars-sinai.org

Spectrum News 1: Cedars-Sinai Researchers Create New AI-Based System to Read Echocardiograms

Cedars-Sinai cardiologist David Ouyang told Spectrum News 1 about a new AI tool that can read echoca...

Cedars-Sinai Medical Center· Original source
🌍Regulatoryispe.org

Bioprocess Online Covers Novo Nordisk Feature at the 2026 ISPE Facilities of the Future Conference

During a sustainability panel at the 2026 ISPE Facilities of the Future Conference, Larry Lane and J...

ISPE (International Society for Pharmaceutical Engineering)· Original source
🇺🇸Industrybiomarin.com

An Open Letter to the Pompe and Fabry Communities

Learn more about BioMarin's origin story and longstanding commitment to rare diseases in this open l...

BioMarin Pharmaceutical· Original source
🇺🇸Industrygsk.com

View latest results

Stiefel (GSK)· Original source
🌍Regulatoryfda.gov.tw

公告115年度「國家藥物科技研究發展獎」自公告日起至115年6月30日止受理申請。

公告115年度「國家藥物科技研究發展獎」自公告日起至115年6月30日止受理申請。

TFDA Taiwan· Original source
🌍Industryorionpharma.com

Medicine deliveries continue despite the conflict in the Middle East3/27/2026 Orion Pharma and Society

Global supply chains have remained resilient despite the escalating conflict in the Middle East. Whi...

Orion Corporation· Original source
🇺🇸Industryir.ideayabio.com

IDEAYA Biosciences Announces Inducement Grants under Nasdaq Listing Rule 5635(c)(4)

IDEAYA Biosciences, Inc. (NASDAQ: IDYA), a precision medicine oncology company committed to the disc...

IDEAYA Biosciences· Original source
🇯🇵Industryotsuka.co.jp

27 MAR 2026PharmaceuticalsOtsuka Pharmaceutical to Acquire Transcend Therapeutics - Expands Otsuka portfolio in psychiatric and neurological fields and aims to accelerate development of Transcend’s portfolio, including the TSND-201 program for post-traumatic stress disorder (PTSD)

Otsuka Pharmaceutical Co., Ltd News Releases

Otsuka Pharmaceutical· Original source
🇯🇵Industryotsuka.co.jp

27 MAR 2026PharmaceuticalsOtsuka Submits Application in Japan for Iclusig®for First-Line Treatment of Philadelphia Chromosome-Positive Acute Lymphoblastic Leukemia

Otsuka Pharmaceutical Co., Ltd News Releases

Otsuka Pharmaceutical· Original source
🇮🇳Regulatorypib.gov.in

PharmaMed 2026 का समापन

Press Information Bureau (PIB) is the nodal agency of the Government of India to disseminate informa...

PIB India Healthcare· Original source
🇺🇸Industryzoetis.com

Feature Stories

Zoetis is a global animal health company dedicated to supporting customers and their businesses in e...

Zoetis· Original source
🇩🇪Regulatoryvfa.de

27.03.2026 [PM 007/26]Mehr Frauenerwerbstätigkeit stärkt Arbeitsmarkt und WachstumDeutschland ist so fleißig wie nieMehr Frauenerwerbstätigkeit stärkt FachkräftebasisTeilzeit, weibliche Führungskräfte und Vergütung sind...

Mehr Frauenerwerbstätigkeit stärkt Arbeitsmarkt und Wachstum Mehr Frauenerwerbstätigkeit stärkt Fach...

VFA Germany· Original source
🇩🇰Industrybavarian-nordic.com

Bavarian Nordic Submits Data to EMA to Extend Mpox and Smallpox Vaccine Approval to Children Aged 2-11 Years

Bavarian Nordic· Original source
🇮🇪Industryir.prothena.com

Irish Statutory Financial Statements

Investors - Financials & Filings - Irish Statutory Financial Statements | Prothena Corporation plc

Prothena· Original source
🌍Industrygedeonrichter.com

20260327 Whc Reg

Gedeon Richter Investors Announcements Richter receives European Commission approval for FYLREVY® (E...

Gedeon Richter· Original source
🇺🇸Regulatoryfda.gov

FDA Approves First Gene Therapy for Severe Leukocyte Adhesion Deficiency Type I

The U.S. Food and Drug Administration today approved Kresladi (marnetegragene autotemcel), the first...

FDA News· Original source
🇺🇸Regulatoryfda.gov

Over-The-Counter Monograph Drug User Fee Program (OMUFA)

A user fee program for nonprescription (over-the-counter or OTC) monograph drugs would be a potentia...

FDA Drug Approvals· Original source
🇬🇧Regulatorygov.uk

Guidance: Archiving and retention of clinical trial records

Information on clinical trial record retention and archiving requirements including requirements for...

MHRA UK· Original source
🇬🇧Regulatorygov.uk

Clinical trials for medicines: good manufacturing practice and radiopharmaceutical investigational medicinal products

Guidance on good manufacturing practice and the use of radiopharmaceutical investigational medicinal...

MHRA UK· Original source
🌍Regulatoryravimiamet.ee

Accelerated assessment procedures support the conduct of drug trials in Estonia and Europe

The State Agency of Medicines has established a national accelerated assessment procedure and is als...

SAM Estonia· Original source
🇬🇧Regulatorygov.uk

Transparency data: MHRA Performance Data

Performance data for MHRA key performance indicators (KPIs) and information on the expected timeline...

MHRA UK· Original source
🇺🇸Researchpubmed.ncbi.nlm.nih.gov

Sevabertinib in Advanced HER2-Mutant Non-Small-Cell Lung Cancer. Reply

PubMed NEJM RSS· Original source
🇺🇸Researchpubmed.ncbi.nlm.nih.gov

Sacituzumab Govitecan in Advanced Triple-Negative Breast Cancer. Reply

PubMed NEJM RSS· Original source
🇺🇸Researchpubmed.ncbi.nlm.nih.gov

Phase 1 Trial of CRISPR-Cas9 Gene Editing Targeting ANGPTL3. Reply

PubMed NEJM RSS· Original source
🇺🇸Researchpubmed.ncbi.nlm.nih.gov

Phase 1 Trial of CRISPR-Cas9 Gene Editing Targeting ANGPTL3

PubMed NEJM RSS· Original source
🇬🇧Researchpubmed.ncbi.nlm.nih.gov

New WHO recommendations for tuberculosis diagnosis

PubMed Lancet Infectious Diseases RSS· Original source
🇬🇧Researchpubmed.ncbi.nlm.nih.gov

Methodological quality assessment tool for observational studies comparing treatment effectiveness in infectious diseases: a Delphi consensus and application to studies on bloodstream infections due to carbapenem-resistant Enterobacterales

PubMed Lancet Infectious Diseases RSS· Original source
🇺🇸Researchpubmed.ncbi.nlm.nih.gov

Final Efficacy and Safety Data From the Phase I/II ARROW Study of Pralsetinib in Patients With Advanced RET Fusion-Positive Non-Small Cell Lung Cancer

PubMed Journal of Clinical Oncology RSS· Original source
🇺🇸Researchpubmed.ncbi.nlm.nih.gov

Old Dog, New Tricks: Oxybutynin for the Treatment of Androgen Deprivation Therapy-Related Vasomotor Symptoms

PubMed Journal of Clinical Oncology RSS· Original source
🇺🇸Researchpubmed.ncbi.nlm.nih.gov

Targeting enhancer RNAs to silence transcription

PubMed Blood RSS· Original source
🇺🇸Researchpubmed.ncbi.nlm.nih.gov

Benchmarking clonal hematopoiesis in sickle cell disease

PubMed Blood RSS· Original source
🇺🇸Researchpubmed.ncbi.nlm.nih.gov

Mandato E, Yan Q, Ouyang J, et al. MYD88L265P augments proximal B-cell receptor signaling in large B-cell lymphomas via an Interaction with DOCK8. Blood. 2023;142(14):1219-1232

PubMed Blood RSS· Original source
🇩🇰Industrylundbeckfonden.com

The Lundbeck Foundation Annual Report 2025

In 2025, the Lundbeck Foundation delivered strong financial results and maintained a high level of g...

Lundbeckfonden (News)· Original source
🇪🇸Regulatoryaemps.gob.es

OMNIPAQUE 300 mg, OMNIPAQUE 350 mg Iodo /ml SOLUCION INYECTABLE y VISIPAQUE 320 mg /ml SOLUCION INYECTABLE

Formato pdf Fecha de publicación: 26 de marzo de 2026 Nº alerta: R_16/2026 Fecha: 25 de marzo de 202...

AEMPS (Spain)· Original source
🇪🇸Regulatoryaemps.gob.es

La AEMPS informa de la detección de un lote falsificado de cánulas nasales con conexión luer-lock para adultos

Generar PDF Fecha de publicación: 26 de marzo de 2026 Categoría: productos sanitarios, productos fal...

AEMPS (Spain)· Original source
🇧🇪Industryglpg.com

Galapagos Announces Nomination of Gino Santini to its Board of Directors

Galapagos (News)· Original source
🇧🇪Industryglpg.com

Galapagos Publishes 2025 Annual Report and Announces Annual and Extraordinary Shareholders’ Meetings

Galapagos (News)· Original source