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Crystal Pharmatech Launches OEB4/OEB5 High-Potency Laboratory, Expanding Global CDMO Capabilities for Complex Drug Development
TelAve News/10894569
New Suzhou facility complements existing U.S. infrastructure, delivering dual-continent containment capabilities for high-potency API programs
SUZHOU, China - TelAve -- Crystal Pharmatech, a global leader in solid-state and formulation science, today announced the official launch of its new OEB4/OEB5 high-potency laboratory at its headquarters in Suzhou, China. The facility has successfully passed rigorous third-party exposure control testing and is now fully operational.
The state-of-the-art laboratory features full-room negative pressure containment, dedicated gowning areas, an independent exhaust system, and five high-performance isolators compliant with ISPE standards and JG/T385:2012. It is equipped with advanced instrumentation including XRPD, TGA, DSC, and high-precision analytical balances to support safe solid-state research and crystallization under containment.
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This new Suzhou facility complements Crystal Pharmatech's existing OEB4/OEB5 capabilities at its U.S. site in Cranbury, New Jersey, creating seamless dual-continent support for highly potent APIs (HPAPIs), including oncology and targeted small-molecule therapies.
Clients can now access integrated early-stage services such as Mol2Med™ Developability Assessment, polymorph screening, solid-state characterization, single crystal structure determination, preformulation, and small-scale crystallization process development (≤20 g) in a fully contained environment.
The expansion strengthens Crystal Pharmatech's position as a trusted global CDMO partner, helping biotech companies reduce development risks, accelerate timelines, ensure operator safety, and advance complex drug programs with confidence.
About Crystal Pharmatech
Crystal Pharmatech provides end-to-end solid-state and formulation solutions from preclinical to clinical stages, with operations in China, the United States, and Canada.
The state-of-the-art laboratory features full-room negative pressure containment, dedicated gowning areas, an independent exhaust system, and five high-performance isolators compliant with ISPE standards and JG/T385:2012. It is equipped with advanced instrumentation including XRPD, TGA, DSC, and high-precision analytical balances to support safe solid-state research and crystallization under containment.
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This new Suzhou facility complements Crystal Pharmatech's existing OEB4/OEB5 capabilities at its U.S. site in Cranbury, New Jersey, creating seamless dual-continent support for highly potent APIs (HPAPIs), including oncology and targeted small-molecule therapies.
Clients can now access integrated early-stage services such as Mol2Med™ Developability Assessment, polymorph screening, solid-state characterization, single crystal structure determination, preformulation, and small-scale crystallization process development (≤20 g) in a fully contained environment.
The expansion strengthens Crystal Pharmatech's position as a trusted global CDMO partner, helping biotech companies reduce development risks, accelerate timelines, ensure operator safety, and advance complex drug programs with confidence.
About Crystal Pharmatech
Crystal Pharmatech provides end-to-end solid-state and formulation solutions from preclinical to clinical stages, with operations in China, the United States, and Canada.
Source: Crystal Pharmatech Co., Ltd.
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