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Company Deals Medical Device PIC

Johnson & Johnson MedTech and CED Medical Sign Third Strategic Cooperation Agreement to Expand Neurointerventional Partnership Behind Qiangyida Stent

Fineline Cube Sep 1, 2026
Company Deals PIC

WestGene and CREATE Sign License Deal to Co‑Develop In Vivo CAR‑T Therapies

Fineline Cube Aug 31, 2026
Company Deals PIC

Simnova Closes nearly RMB 400 Million Series B to Advance CAR‑NK Candidate SNC103

Fineline Cube Aug 31, 2026
Company Deals PIC

Leaderna Therapeutics Closes Series A+ Led by Grand View Capital to Advance Oligonucleotide Pipeline

Fineline Cube Aug 31, 2026
Company Drug PIC

Eli Lilly Wins FDA Approval for Mounjaro Cardiovascular Risk Reduction in Type 2 Diabetes

Fineline Cube Aug 31, 2026
Company Deals Medical Device PIC

Johnson & Johnson MedTech and CED Medical Sign Third Strategic Cooperation Agreement to Expand Neurointerventional Partnership Behind Qiangyida Stent

Fineline Cube Sep 1, 2026
Policy / Regulatory

NMPA CDE Issues Draft Guideline to Reduce or Replace Animal Testing for Monoclonal Antibodies, Opening Public Comment

Fineline Cube Sep 1, 2026
Company Policy / Regulatory

Shanghai RAAS’s SR604 Enters NMPA CDE Rare Disease Encouragement Program for Hemophilia and Factor VII Deficiency Treatment

Fineline Cube Sep 1, 2026
Company Deals

Broncus Medical and Hangzhou Norchant Terminate Licensing Agreement with Cancellation Fee

Fineline Cube Nov 27, 2023

Broncus Medical Inc., (HKG: 2216) a provider of lung disease precision intervention solutions with operations...

Company

FDA Raises Concerns Over Research Conditions at Roche’s Genentech Trial Site

Fineline Cube Nov 27, 2023

The US Food and Drug Administration (FDA) has voiced concerns regarding the research conditions at...

Company Drug

Jiangxi Jemincare Group Secures NMPA Approval for Generic Ibrance Capsules

Fineline Cube Nov 27, 2023

Jiangxi Jemincare Group, a Chinese pharmaceutical company, has announced that it has received market approval...

Policy / Regulatory R&D

China’s CDE Releases Draft Guidelines for Decentralized Trials in Rare Disease Drug Development

Fineline Cube Nov 27, 2023

China’s Center for Drug Evaluation (CDE) has released draft “Technical Guidelines for the Application of...

Company Legal / IP

AbbVie Sues to Protect Rinvoq from Generic Competition in the US Market

Fineline Cube Nov 27, 2023

AbbVie (NYSE: ABBV) has initiated legal action in the US to safeguard its blockbuster drug...

Company Drug

Novo Nordisk Sets February 2024 Launch for Wegovy in Japan, Expanding into Asia

Fineline Cube Nov 27, 2023

Novo Nordisk (CPH: NOVO-B), headquartered in Denmark, has announced that it will launch its anti-obesity...

Company Drug

Jiangsu Hengrui Pharmaceuticals Receives NMPA Approval for Phase Ib/II Study of Dalpiciclib and HRS-8080

Fineline Cube Nov 24, 2023

China-based Jiangsu Hengrui Pharmaceuticals Co., Ltd. (SHA: 600276) has announced that it received approval from...

Company Drug

Fosun Pharmaceutical Gets FDA Green Light for HLX42 ADC Clinical Study

Fineline Cube Nov 24, 2023

Fosun Pharmaceutical (Group) Co., Ltd (HKG: 2196; SHA: 600196) has received approval from the US...

Company Deals

Simcere Pharmaceutical Secures Rights to Develop Rademikibart in China

Fineline Cube Nov 24, 2023

China’s Simcere Pharmaceutical Co., Ltd (HKG: 2096) has entered into an agreement to acquire the...

Company

Bayer Invests USD 130 Million in Parenteral Drugs Manufacturing Site in Germany

Fineline Cube Nov 24, 2023

Bayer (ETR: BAYN) has inaugurated a new state-of-the-art parenteral drugs manufacturing site at its German...

Company

Novo Nordisk Invests DKK 16 Billion to Expand French Production Facility

Fineline Cube Nov 24, 2023

Denmark-based pharmaceutical giant Novo Nordisk (CPH: NOVO-B) has initiated an expansion of its production facility...

Company Deals

Shanghai Escugen Partners with Foreseen Biotechnology for ADC Development

Fineline Cube Nov 24, 2023

China-based Shanghai Escugen has entered into a partnership with domestic firm Foreseen Biotechnology to develop...

Policy / Regulatory

European Commission Proposes Overhaul of Pharmaceutical Legislation

Fineline Cube Nov 24, 2023

The European Commission (EC) is advancing an update to Europe’s 20-year-old pharmaceutical legislation, with the...

Company Drug

Pyrotech Biotechnology’s PTT-936 Gets US FDA Clinical Trial Approval

Fineline Cube Nov 24, 2023

Pyrotech (Beijing) Biotechnology Co., Ltd, a China-based biotech firm, has announced that it has received...

Company Drug

Boehringer Ingelheim and Eli Lilly’s Jardiance Receives NMPA Approval for CKD Treatment

Fineline Cube Nov 24, 2023

Boehringer Ingelheim (BI) and Eli Lilly (NYSE: LLY) have announced that their SGLT2 inhibitor, Jardiance...

Company Deals

Zhejiang Huanqing Medical Technology Secures Series A Financing for Heart Failure Innovations

Fineline Cube Nov 24, 2023

Zhejiang Huanqing Medical Technology Co., Ltd, a Chinese specialist in heart failure solutions, has reportedly...

Company Drug

Boehringer Ingelheim and Eli Lilly Secure NMPA Approval for Jardiance in Chronic Kidney Disease

Fineline Cube Nov 24, 2023

Boehringer Ingelheim (BI) and Eli Lilly (NYSE: LLY) have announced the receipt of marketing approval...

Company Deals

True Health Secures Over RMB 100 Million in Series B+ Financing for Surgical Robot Development

Fineline Cube Nov 24, 2023

True Health, a Guangdong-based surgical robot developer backed by Gree Group, has reportedly raised over...

Company Drug

MicuRx Pharmaceuticals Secures NMPA Approval for MRX-4 and Contezolid Combination Therapy

Fineline Cube Nov 24, 2023

Sino-US firm MicuRx Pharmaceuticals Inc. has announced that it has received clinical trial approval from...

Company Deals

Stada Arzneimittel AG Partners with CR Sanjiu for Distribution in China

Fineline Cube Nov 24, 2023

Germany-based Stada Arzneimittel AG has announced a strategic distribution and promotion partnership with China’s state-owned...

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Recent updates

  • NMPA CDE Issues Draft Guideline to Reduce or Replace Animal Testing for Monoclonal Antibodies, Opening Public Comment
  • Shanghai RAAS’s SR604 Enters NMPA CDE Rare Disease Encouragement Program for Hemophilia and Factor VII Deficiency Treatment
  • Eisai Launches LEQEMBI IQLIK Subcutaneous Auto-Injector for Early Alzheimer’s Disease in the United States
  • Trump Signs Nine New MFN Drug Pricing Agreements, Expanding Pharma Deals to 26 Companies Covering 89% of Branded Market
  • Laekna Doses First Patient in Phase I Study of LAE118 PI3Kα Inhibitor for Advanced Solid Tumors, Licensed to Vasque Bio for Up to USD 527 Million
Special Report 2025 Q1: U.S. Targets Chinese Pharma with 200% Tariffs—Will the Global Drug Market Collapse?

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You Missed

Policy / Regulatory

NMPA CDE Issues Draft Guideline to Reduce or Replace Animal Testing for Monoclonal Antibodies, Opening Public Comment

Company Policy / Regulatory

Shanghai RAAS’s SR604 Enters NMPA CDE Rare Disease Encouragement Program for Hemophilia and Factor VII Deficiency Treatment

Company Drug

Eisai Launches LEQEMBI IQLIK Subcutaneous Auto-Injector for Early Alzheimer’s Disease in the United States

Policy / Regulatory

Trump Signs Nine New MFN Drug Pricing Agreements, Expanding Pharma Deals to 26 Companies Covering 89% of Branded Market

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