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CHEMILL: 25 Years of Empowering Generic Drug Manufacturers For the past 25 years, we at CHEMILL Group have been a trusted partner to generic drug manufacturers, committed to empowering them with comprehensive services that span the entire spectrum of the drug development process. From API sourcing to the market access of finished dosage forms (FDFs), we have been at the forefront of supporting generic drug companies in creating value and navigating the complex pharmaceutical landscape. We offer the following comprehensive services to generic drug manufacturers:
1. API Sourcing and Supply: Our procurement specialists leverage their extensive global network to source high-quality raw materials, ensuring a smooth and cost-effective supply chain for our clients.
2. Dossier Development for In-licensing: Our team of regulatory experts specializes in preparing comprehensive dossiers for in-licensing opportunities, ensuring that our clients' products meet the stringent requirements of target markets.
3. Finished Dosage Form (FDF) Manufacturing: We partner with leading FDF manufacturers worldwide, providing our clients with access to state-of-the-art production facilities and cutting-edge technologies. We oversee the entire manufacturing process, from formulation development to packaging, guaranteeing the highest quality standards.
4. Streamlined Operations and Efficiency: By leveraging our industry knowledge and global connections, we help generic drug manufacturers streamline their operations and enhance overall efficiency.
5. Driving Innovation in the Generic Drug Sector: We continuously invest in research and development to identify new opportunities for growth, enabling our clients to stay ahead of the curve and offer cutting-edge generic drug solutions.
6. Market Access Services: We provide comprehensive market access services to help generic drug manufacturers expand into new markets and create value. By leveraging our expertise in regulatory compliance, product registration, and supply chain management, we enable our clients to navigate the complexities of international markets and accelerate their speed to market. In summary, our 25 years of experience and comprehensive suite of services cover the entire spectrum of the generic drug development process, from API sourcing to market access. By empowering generic drug manufacturers and providing market access services, we have been instrumental in creating value and driving innovation in the industry.
康美尔:25年来推动仿制药企业创造价值 .
25年来,康美尔集团一直是仿制药制造商值得信赖的合作伙伴,致力于为他们提供整个药物开发过程及打造全方位服务。从原料药(API)采购到成品剂型(FDF)的市场准入,康美尔集团一直处于支持仿制药企业创造价值和应对复杂制药行业挑战的前沿。 我们为仿制药制造商提供以下全面的服务:
1. **API采购与供应**:我们的采购专家利用广泛的全球网络,为客户采购高质量的原料药,确保供应链顺畅高效。
2. **用于引进许可的申报文件开发**:我们的监管专家擅长为引进许可的机会准备全面的申报文件,确保客户的产品满足目标市场的严格要求。
3. **成品剂型(FDF)制造**:我们与全球领先的FDF制造商合作,为客户提供先进的生产设施和尖端技术。我们全程参与从配方开发到包装的整个制造过程,确保最高的质量标准。
4. **提高运营效率**:凭借我们的行业知识和全球联系,我们帮助仿制药制造商优化运营,提高整体效率。
5. **推动仿制药行业创新**:我们不断投资研发,发掘新的增长机会,使我们的客户保持领先地位,提供尖端的仿制药解决方案。
6. **市场准入服务**:我们提供全面的市场准入服务,帮助仿制药制造商拓展新市场,创造价值。通过利用我们在监管合规、产品注册和供应链管理方面的专业知识,我们使客户能够应对国际市场的复杂性,加快进入市场的速度。 总之,我们25年的经验和全面的服务组合涵盖了整个仿制药开发过程,从API采购到市场准入。通过赋能仿制药制造商并提供市场准入服务,康美尔集团一直在推动行业创新,帮助企业创造价值。
Year of Establishment: 2023
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Main Competitive Advantages: Brand Name,International Approvals/Standards,Large Product Line
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