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以创新为翼 着力培育生物医药产业新质生产力
Xin Hua Ri Bao·2025-05-21 22:19

Core Viewpoint - Zhuohe Pharmaceutical Group Co., Ltd. is a comprehensive enterprise focusing on drug research and development, sales, and marketing authorization holder (MAH), with a strategy that combines raw materials and formulations, innovative drugs, and specialty generics, aiming for both domestic and global markets [1] Group 1: Talent and Innovation - Talent is a strong driving force for innovation in the biopharmaceutical sector, and the company has implemented a comprehensive employee quality improvement system, including business training and skill competitions [2] - The company has established a "1+1" mentor training model to cultivate young talents and has recognized several individuals as high-level innovative talents at various governmental levels [2] - The head of the R&D analysis department has led the team to overcome challenges in multiple new drug projects and has been recognized for her contributions, including a national invention patent [2] Group 2: Innovation System - The company emphasizes that R&D innovation is the source of its development and has established several provincial-level research centers and specialized R&D platforms [3] - Currently, the company has over 70 ongoing research projects in various disease areas and has received 22 domestic and international invention patents, with over 100 patent applications filed [3] - Notable achievements include the approval of a traditional Chinese medicine innovative drug and the advancement of a new generation JAK1 selective inhibitor into phase III clinical trials [3] Group 3: Global Market Expansion - Zhuohe Pharmaceutical is actively expanding its international business, with 13 raw material products certified in major markets, including the U.S., EU, and Japan [4] - The company has achieved significant market presence, with its raw material product, Neomycin sulfate, holding over 50% of the global high-end market [4] - Recent milestones include FDA registration for its oral formulation workshop and the approval of a new drug application for a specific capsule, marking entry into mainstream international markets [4]