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Stonycreek Pharmatech Co., Ltd. is a trusted global partner in the development and manufacturing of high-purity pharmaceutical intermediates and active pharmaceutical ingredients (APIs). Committed to cGMP standards, we deliver reliable, scalable, and compliant solutions for the evolving healthcare landscape.
A leader in pharmaceutical development and manufacturing, dedicated to quality, innovation, and customer success.
Stonycreek Pharmatech Co., Ltd. is a research-driven pharmaceutical company specializing in the synthesis and production of high-purity intermediates and active pharmaceutical ingredients (APIs). With a strong foundation in organic chemistry and process optimization, we support pharmaceutical innovators across North America, Europe, and Asia.
Our state-of-the-art facilities adhere to current Good Manufacturing Practices (cGMP) and are equipped with advanced analytical instrumentation to ensure product consistency, purity, and regulatory compliance. We focus on scalable processes that transition seamlessly from lab-scale development to commercial production.
Manufacturing under strict quality systems aligned with international regulatory standards.
Tailored development and production of complex molecules for clinical and commercial use.
High-purity intermediates and APIs developed with precision for reliability and performance.
Key building block for DPP-4 inhibitors used in type 2 diabetes treatment.
Critical intermediate for antiviral agent used in CMV prophylaxis.
High-purity intermediate for third-generation EGFR inhibitor in oncology.
Key compound for multimodal antidepressant therapy.
Intermediate for soluble guanylate cyclase stimulator used in heart failure.
JAK1-selective inhibitor intermediate for autoimmune disease therapeutics.
Peptide fragment used in the synthesis of GLP-1 analogs for diabetes and obesity.
End-to-end development and manufacturing of novel APIs under cGMP.
From discovery to delivery, we offer comprehensive services to accelerate your drug development.
Fully compliant production with rigorous quality control and documentation.
Optimization of synthetic routes for yield, purity, safety, and scalability.
Comprehensive testing using HPLC, GC, NMR, MS, and residual solvent analysis.
Efficient project management and rapid delivery timelines for urgent needs.
Find answers to common inquiries about our services and products.
We specialize in high-purity pharmaceutical intermediates and active pharmaceutical ingredients (APIs), including custom synthesis for clinical and commercial use. Our portfolio includes intermediates for diabetes, oncology, antiviral, and CNS therapeutics.
Yes, our manufacturing facilities operate under current Good Manufacturing Practices (cGMP) with robust quality systems, documentation, and validation protocols to meet international regulatory requirements.
Absolutely. We offer end-to-end custom synthesis services, from route scouting and process development to scale-up and commercial manufacturing, with full regulatory support.
Lead times vary based on complexity and scale, but we typically deliver kilogram-scale intermediates within 6–10 weeks. Expedited timelines are available upon request.
Yes, each batch is accompanied by a Certificate of Analysis (CoA) including HPLC, NMR, MS, and residual solvent data, along with full traceability and batch records.
Contact Stonycreek Pharmatech to discuss your next pharmaceutical development project.
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