PharmaBlock has established a fully integrated CDMO service platform to support global partners in accelerating drug development, reducing R&D and production costs, and fostering greener, more sustainable pharmaceutical manufacturing. The company is dedicated to delivering efficient and high-quality development and manufacturing services for drug substances and drug products, covering all stages from development to commercialization.

In the realm of API, intermediate, and RSM development and manufacturing, PharmaBlock has developed a robust suite of CMC competencies. By capitalizing on its quick access to building blocks as raw materials, accumulated chemistry know-how and low-carbon technologies, the company has been earning increasing trust and recognition from global partners.

• Development and manufacturing solutions for drug substances and drug products throughout the development and commercial stages
• Well established Quality, EHS and IP protection system
• Professional project management and delivery teams
• GMP manufacturing facility (FDA GMP inspected with no Form 483s issued, passed NMPA PAIs)

• Innovative route scouting for fast delivery and cost control
• Accumulated chemistry know-how for challenging molecules

• Enable safer, greener and more efficient solutions for development & manufacturing
• Click here for more information about the chemistry and engineering technology platform

• Flexible supply management and cost control of building blocks as raw materials
• Robust supplier development program to ensure sustainable key materials supply
• Multiple operation sites in US & China to fortify a resilient supply chain

• Optimal route scouting
• FFS and FTE for process R&D of RSMs, intermediates, APIs
• Impurity studies and synthesis
• Solid State Chemistry
• Analytical development & quality control
• cGMP manufacturing of intermediates and APIs
• CMC regulatory filing support