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Company Deals

WuXi XDC Licenses WuXiTecan-2 Technology to Earendil Labs – $885M Deal Powers AI‑Driven ADC Development

Fineline Cube Feb 27, 2026
Company Deals

SteinCares Partners with Shilpa Biologicals on Latin America Biosimilar Deal – Regional Commercialization Agreement

Fineline Cube Feb 26, 2026
Company Deals

Danaher to Acquire Masimo for $9.9B – Expands Diagnostics Platform with Pulse Oximetry Leader

Fineline Cube Feb 26, 2026
Company Deals

Novo Nordisk Partners with Vivtex on $2.1B Oral Biologics Deal – Targets Obesity and Diabetes Delivery Innovation

Fineline Cube Feb 26, 2026
Company Deals

GSK to Acquire 35Pharma for $950M – Adds Potential Best‑in‑Class PAH Asset HS235

Fineline Cube Feb 26, 2026
Policy / Regulatory

NMPA Approves 76 Innovative Medical Devices in 2025 – 17% YoY Growth Driven by AI and Priority Review Surge

Fineline Cube Feb 26, 2026
Company Drug

FDA Approves Boehringer’s Zongertinib in Record 44 Days – First Oral HER2 TKI Wins CNPV Fast‑Track

Fineline Cube Feb 27, 2026
Company Drug

Fosun Pharma’s Luvometinib Cleared for Phase II NSCLC Combination Trial – MEK Inhibitor Plus Anlotinib Targets KRAS Mutations

Fineline Cube Feb 26, 2026
Company Drug

Brii Biosciences’ HBV Drug Candidates Receive NMPA’s Breakthrough Therapy Designations

Fineline Cube May 14, 2024

Brii Biosciences Ltd (HKG: 2137) has announced that two of its hepatitis B virus (HBV)...

Company Drug

HutchMed’s HMPL-306 Advances to Phase III Trial in R/R AML Patients

Fineline Cube May 14, 2024

HutchMed (China) Ltd (NASDAQ: HCM; HKG: 0013) has announced the commencement of the RAPHAEL study,...

Company Drug

Zai Lab’s ROS1 Inhibitor Augtyro Earns NMPA Nod for Advanced NSCLC Treatment

Fineline Cube May 13, 2024

Zai Lab Ltd (NASDAQ: ZLAB; HKG: 9688), a biopharmaceutical company based in China, has announced...

Company Drug Medical Device

NMPA Accepts Jiangsu Yahong Meditech’s Application for Cervical HSIL Treatment Cevira

Fineline Cube May 13, 2024

Jiangsu Yahong Meditech Co., Ltd (Asieris, SHA: 688176), a specialist in urogenital cancer treatments in...

Company Drug

Mabwell’s 9MW2821 ADC for Triple Negative Breast Cancer Accepted for Review by NMPA

Fineline Cube May 13, 2024

Mabwell (Shanghai) Bioscience Co., Ltd (SHA: 688062), a biopharmaceutical company based in China, has announced...

Company Drug

Huadong Medicine’s EGFR Inhibitor Mefatinib for NSCLC Accepted by NMPA for Review

Fineline Cube May 13, 2024

Huadong Medicine Co., Ltd (SHE: 000963), a leading pharmaceutical company based in China, has announced...

Company Deals Medical Device

Subtle Medical Inc Closes USD 10 Million Series B+ Round to Accelerate Global Expansion

Fineline Cube May 13, 2024

Subtle Medical Inc, a medical imaging specialist and Stanford University spin-off, has reportedly raised close...

Company Drug

Shenzhen Hepalink’s Enoxaparin Sodium Gets Green Light in Singapore

Fineline Cube May 13, 2024

Shenzhen Hepalink Pharmaceutical Group Co., Ltd (SHE: 002399), a leading pharmaceutical company based in China,...

Policy / Regulatory

NMPA Updates In Vitro Diagnostic Reagents Classification List for Enhanced Regulatory Oversigh

Fineline Cube May 13, 2024

The National Medical Products Administration (NMPA) has coordinated the revision and release of the In...

Company Deals

Novartis Inks Deal to Acquire Mariana Oncology, Bolstering Radioligand Therapy Portfolio

Fineline Cube May 13, 2024

Swiss pharmaceutical giant Novartis (NYSE: NVS) is poised to expand its oncology portfolio by acquiring...

Policy / Regulatory

China’s NMPA Revamps Medical Device Classification Rules to Improve Regulatory Efficiency

Fineline Cube May 13, 2024

The National Medical Products Administration (NMPA) has revised the “Notice on Standardizing the Classification of...

Company Drug

BMS’s Opdivo/Yervoy Combo Misses PFS Endpoint in Unresectable Stage III NSCLC Trial

Fineline Cube May 13, 2024

Bristol-Myers Squibb (BMS; NYSE: BMY) has announced that a late-stage trial for its checkpoint inhibitors...

Company Drug

FDA Reviews BMS’ Opdivo Subcutaneous Formulation for Broad Indications

Fineline Cube May 13, 2024

The US Food and Drug Administration (FDA) has agreed to review a submission from Bristol-Myers...

Company Policy / Regulatory

BIO Survey Highlights Extensive Dependence on Chinese CDMOs in Life Sciences

Fineline Cube May 11, 2024

The Biotechnology Innovation Organization (BIO), a US industry trade group, has completed a survey among...

Company Drug

Yunnan Baiyao’s Radiopharmaceutical INR101 Advances to Clinical Trial Stage with NMPA Approval

Fineline Cube May 11, 2024

Yunnan Baiyao Group Co., Ltd (SHE: 000538), a traditional Chinese medicine (TCM) company based in...

Company Drug

Eisai’s Fycompa Gains New Indication for Generalized Tonic-Clonic Seizures in China

Fineline Cube May 11, 2024

Eisai Co Ltd (TYO: 4523), a Japanese pharmaceutical company, has announced that its antiepilepsy drug...

Company Deals

Ribobay Pharma and General Biol to Commence GMP-Grade Oligonucleotide Manufacturing Services

Fineline Cube May 11, 2024

Shanghai-based contract research, development, and manufacturing organization (CRDMO) Ribobay Pharma has announced plans to commence...

Company Policy / Regulatory

BioSecure Act Advances in US, Aiming to Curb Ties with Chinese Bioscience Firms

Fineline Cube May 11, 2024

US legislators are working expeditiously to finalize the BioSecure Act, legislation that, if enacted, would...

Company Drug

Jacobio Pharma’s KRAS G12C Inhibitor Gains NMPA Approval for Phase III CRC Study

Fineline Cube May 11, 2024

Jacobio Pharma (HKG: 1167), a biopharmaceutical company based in China, has announced that it has...

Company Deals

Tianjin Lisheng Pharmaceutical Co., Ltd. to Sell Stake in Mitsubishi Tanabe’s China Subsidiary

Fineline Cube May 11, 2024

Tianjin Lisheng Pharmaceutical Co., Ltd. (SHE: 002393), a Chinese pharmaceutical company, has announced plans to...

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Recent updates

  • BeOne Medicines Reports $5.3B Full‑Year Revenue – Brukinsa Drives 40% Growth, 2026 Guidance Raised
  • FDA Approves Boehringer’s Zongertinib in Record 44 Days – First Oral HER2 TKI Wins CNPV Fast‑Track
  • WuXi XDC Licenses WuXiTecan-2 Technology to Earendil Labs – $885M Deal Powers AI‑Driven ADC Development
  • MSD’s Prevymis Wins NMPA Approval for 200‑Day Pediatric CMV Prophylaxis – Extended Post‑Transplant Protection
  • SteinCares Partners with Shilpa Biologicals on Latin America Biosimilar Deal – Regional Commercialization Agreement
Special Report 2025 Q1: U.S. Targets Chinese Pharma with 200% Tariffs—Will the Global Drug Market Collapse?

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You Missed

Company

BeOne Medicines Reports $5.3B Full‑Year Revenue – Brukinsa Drives 40% Growth, 2026 Guidance Raised

Company Drug

FDA Approves Boehringer’s Zongertinib in Record 44 Days – First Oral HER2 TKI Wins CNPV Fast‑Track

Company Deals

WuXi XDC Licenses WuXiTecan-2 Technology to Earendil Labs – $885M Deal Powers AI‑Driven ADC Development

Others

MSD’s Prevymis Wins NMPA Approval for 200‑Day Pediatric CMV Prophylaxis – Extended Post‑Transplant Protection

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