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AGC Chemicals Americas
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Your Reliable CDMO Partner for Small Molecule APIs and HPAPIs
With technical expertise and cGMP facilities worldwide, AGC Pharma Chemicals provides custom synthesis for clinical trials, process R&D, and commercial scale-up of small-molecule APIs, HPAPIs, and intermediates.
We integrate cutting-edge technologies and facilities for our CDMO services in the process development and manufacturing of Active Pharmaceutical Ingredients (APIs) and intermediates. Our infrastructure is purpose-built to deliver services that ensure flexibility, scalability and top pharma quality, enabling us to meet the diverse needs of our clients and bring their pharmaceutical innovations to life.
Supply Chain Management
At AGC Pharma Chemicals, our supply chain is designed to provide flexibility, stability, and on-time delivery across global markets. With a strategic network in key regions —Europe, Japan, India, and China— we offer a seamless, end-to-end supply chain solution that minimizes risks and ensures continuous delivery. Our OTIF (On-Time shipments In Full shipments) rate is 99-100% (from 2020-2024).
CDMO Services
We offer a comprehensive suite of Services & Capabilities and expert teams for your Small Molecule APIs and Intermediates projects. Our strategic network and lean operations enable us to offer flexible capacity and end-to-end services without compromising on quality, resulting in competitive costs that benefit our clients worldwide. From innovative Process Development and reliable API Life Cycle Management to rigorous Quality Management and an optimized Supply Chain, we ensure that your projects receive the attention and expertise they deserve at every stage of their journey to market success.
Facilities
We have a global presence with strategically located cGMP manufacturing plants in Japan and Spain (Barcelona).
AGC Pharma Chemicals Website
Click here to visit AGC Pharma Chemicals, which has more information about global CDMO services for small molecule active pharmaceutical ingredients and intermediates.
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Delivering Top Pharma Quality
- End-to-End Solutions & Scale-Up – Lab-scale R&D to commercial production (up to OEB5).
- cGMP-Compliant Manufacturing – Global regulatory standards with full batch documentation and a proven track record of successful inspections and commercial launches.
- Flexible, Customer-Focused Solutions – Custom processes within technical and regulatory scope.
- Robust Quality & Analytical Support – Advanced testing, impurity profiling, and batch release.
- Reliable & Scalable Production – From grams to tons, supporting global supply chains.
Advanced Technologies and State-of-the-Art Facilities for Agile and Flexible API Process Development and Manufacturing
- R&D center
- cGMP Kilolab
- cGMP Pilot Plant
- cGMP Multi-purpose manufacturing site
- cGMP Micronization plant
- HAPI and HPAPI capabilities
- Fluorination
- Other Special Technologies such us flow chemistry, bromination, cryogenic reactions, hazardous reactions and other general organic reactions.
AGC Pharma Chemicals
Reactor Capacity: 156m3
Both commercial and clinical phase APIs / intermediates
Click here to request an SDS sheet.
Helpful Resources
Contact our experts to discuss your specific needs.
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