GfM is a market-leading contract manufacturer providing cGMP micronization and milling services to the pharmaceutical and chemical industries. Since 1985, we have been dedicated to serving customers worldwide with a 100% commitment to quality. We consistently provide the best solutions for the required particle size distribution through feasibility trials and read moresamples with unique specifications. Our services range from process development to routine production, handling quantities from grams to tons, and include:

• Micronization
• Milling
• Cryogenic Millingv
• Sterile Micronization
• Micronization in Isolator
• Fractionated Sieving
• Homogenization & Blending
• PSD Analysis
• PSD Development, Transfer & Validation

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GlycoSyn is a world-leader in carbohydrate, polymer, pharmaceutical excipient and complex chemistry. We can help you as a contract development and manufacturing organization (CDMO or contract research organization (CRO).

Located in the Gracefield Innovation Quarter in Wellington, New Zealand, we are passionate about creating life-changing drugs. read moreOur experience in current good manufacturing practice (cGMP) means we can help you take your products from concept to the lab and into the clinic. [website]

Grace’s Fine Chemical Manufacturing Services (FCMS) is a leading CDMO in North America, differentiated by extensive expertise and the ability to provide integrated solutions for the pharmaceutical, nutraceutical, and other fine chemical industries.

Our fine chemical offerings enable us to be your fully integrated read moredomestic partner for the development and manufacture of registered starting materials (RSMs), intermediates, and custom active pharmaceutical ingredients (APIs). Not only can we integrate into your RSM, but we can also partner with you from the lab all the way to commercial production, and provide compliance leadership throughout the process.

Grace’s strategically located fine chemical facilities in Pennsylvania, Michigan and Oregon are designed to meet customers’ quality, regulatory and confidentiality expectations. 

Their capabilities include:

• Audited and qualified cGMP environment
• Kilos-to-tonnes custom manufacturing
• Scale-up expertise and technology
• Expanded research and development (R&D) capabilities
• ISO 9001 certification