Clinical and Commercial Manufacturing

Leveraging a robust drug formulation services platform, Crystal Pharmatech is recognized as a reliable partner that delivers high-quality, fast, flexible clinical and commercial production services to meet our customers' different needs, helping them accelerate their drug launches.

Dosage forms

• Solid oral dosage forms (tablet, capsule, sachet)

• Amorphous Solid Dispersions (ASD, Spray Drying & Hot Melt Extrusion) for insoluble compounds & PROTAC & oral peptides 

• Pediatric Dosage Form (mini-tablet)

Crystal Pharmatech  (CDMO Site in China, Crystal Formulation Services)
located in Suzhou, China, our 50,590 sq. ft. facility is designed to support pharmaceutical and manufacturing needs:

• R&D Facility (11,840 sq. ft.) - Dedicated to research and development projects

• GMP Facility (17,250 sq. ft.) - Equipped to handle batch sizes up to 120 kg

• Clinical Supply Depot (21,500 sq. ft.) - Provides packaging, labeling, storage and distribution, with extended support through a partnered U.S. depot

Crystal Pharmatech (CDMO Site in Canada, Candoo Pharmatech)
located in Toronto, Canada, our 12,500 sq. ft. facilities are designed to meet your pharmaceutical and manufacturing needs:

• R&D Facility (3,500 sq. ft.) - Dedicated to research and development projects

• GMP Facility (9,000 sq. ft.) - Equipped to handle batch sizes up to 100 kg

An experienced team with highly efficient execution

The GMP team are experts with extensive industry experience, unique skills in optimizing and troubleshooting production and analysis, and broader chemistry expertise. We ensure that your project gets the focus it needs and with our expertise in technical transfer, we can increase manufacturing efficiency.

World-class manufacturing equipment

Taking advantage of our advanced technologies and world-class manufacturing equipment, Cyrstal Pharmatech is uniquely positioned to deliver high-quality drug products to achieve or beyond your goals.

cGMP and QMS meeting NMPA, FDA, and EMA requirements

Crystal Pharmatech’s infrastructure, quality systems, and verification and validation procedures comply with international cGMP standards, laying a solid foundation for us to provide CDMO services that meet the FDA, NMPA, and EMA regulations.