Connecting You with Health Support
We're dedicated for better health!
Connecting You with Health Support
We're dedicated for better health!
Insights
Pharmaceutical Manufacturing
Embodied Regulatory Intelligence
Pharmaceutical Manufacturing
Custom Research & Services
Embodied Regulatory Intelligence
Pharmaceutical Manufacturing
Innovative Research Tools
Embodied Regulatory Intelligence
Embodied Regulatory Intelligence
Embodied Regulatory Intelligence
Embodied Regulatory Intelligence
Embodied Regulatory Intelligence
WHO WE ARE
We Führung Pharma, are a research and innovation-driven company dedicated to offering reliable and efficient pharmaceutical services to our clients across the globe. Our expertise in GMP-compliant manufacturing of drugs and end-to-end custom synthesis (CRO/CDMO/CRAMS) business makes us a trusted partner for pharmaceutical companies navigating the complexities of drug development and manufacturing.
WHAT WE DO
Because of our GMP compliant site, skilled staff, available technologies, and collaborative approach to every project, we can provide end-to-end solutions and support standalone programs. Apart from the manufacturing and CRO/CDMO support, we also have expertise in providing, global regulatory support, material management and GMP compliance
WHY WE
At Führung, we work hard to establish ourselves as a trustworthy development and manufacturing partner. Our ability to offer affordable and effective APIs and Intermediates is made possible by our contract research and manufacturing services (CRAMS). We are a dynamic adaptive team committed to bettering people's lives by accelerating the pace of drug development, discovery and production.
OUR ADVANTAGES
Our strengths include WHO/cGMP-compliant manufacturing site, a robust and secure supply chain, and optimized lead times. We maintain in-house R&D and process development capabilities, as well as dedicated project management and regulatory affairs teams. Our local office in China supports our global reach, and we offer flexible working models, including FTE and FFS arrangements, to meet diverse client needs.
Brief Overview
API Manufacturing and Supply
Leveraging our in-depth knowledge of cutting-edge pharmaceutical technology, trends, and practices, we strive to manufacture Active Pharmaceutical Ingredients (APIs) of the highest quality and purity. Our products are manufactured with ISO, cGMP and WHO GMP accredited facilities and regularly audited to ensure adherence to the strict quality standards
Custom Synthesis (CRO/CDMO/CRAMS)
We offer end-to-end custom synthesis (CRO/CDMO/CRAMS) services across all the categories of active pharmaceutical ingredients (API) and Intermediates during drug discovery, pre-clinical, and generic preparations to meet our customers diversified needs.
Process Chemistry
Our process chemistry services assist clients in achieving their objectives through a comprehensive range of offerings. These include patent screenings, process design, optimization, and improvement, all conducted in accordance with contemporary trends such as Design Space, QbD-DoE (Quality by Design - Design of Experiments), and Quality Risk Assessment.
Global Regulatory
Our regulatory services encompass a wide spectrum, including regulatory strategy intelligence, gap assessments, and comprehensive solutions for the compilation and registration of Drug Master Files (DMFs), dossiers, Biologics License Applications (BLAs), and Medical Device applications globally.
Quality Policy
"Quality embodies the spirit of our organization. it is our strength which is the outcome of continuous innovation through persistent research and development. Quality being our main priority, we have a full-fledged quality and price control department where all the products, procured and manufactured, go through various stringent tests to ensure they meet the quality and consistency standards. We employ the latest technology and techniques for the quality enhancement of our products".