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B4-101, Biobay, 218 Xinghu Street, Suzhou Industrial Park, Suzhou, 215123 China SuZhou, 215123 ChinaEstablished in 2010, Crystal Pharmatech is a specialized CRO/CDMO, excelling in crystal form and formulation services. Our exceptional track record includes supporting 1,000 clients and collaborating on over 2,000 compounds, showcasing our expertise in solid-state research, crystallization, pre-formulation, formulation development, and manufacturing. With a global presence encompassing three strategically located R&D centers in Suzhou (China), New Jersey (USA), and Toronto (Canada), we are powered by a skilled team of around 250 professionals. As a leader in both conventional and enabling formulation technologies, including amorphous solid dispersion, we take pride in our cGMP facilities, strictly adhering to the rigorous standards set by the FDA, EMA, and NMPA. Our integrated service encompasses the entire new drug development journey, from developability assessment and solid form screening to pre-formulation, formulation development, and CTM and commercial manufacturing. Introducing our pioneering Mol2Med program, designed to expedite small molecule lead compounds or preclinical candidates into Phase I and beyond, with unparalleled efficiency and precision. This 3-step First-Time-Right approach begins at the lead optimization/PCC stage: Step 1: Developability Assessment to guide API form selection and formulation design. Step 2: Solid form screening/selection and Preformulation. Step 3: Formulation development and CTM manufacturing, including packaging, labeling, and shipping to the clinical site. This innovative approach guarantees a robust API form and a scalable manufacturing process, culminating in a First-Time-Right formulation for Phase I. Streamlining the transition to future clinical studies upon Phase I success, our First-Time-Right approach sets the foundation for optimized drug development and success beyond. Leveraging its small molecule expertise, material science, and analytical chemistry, Crystal Pharmatech strategically entered the Biologics sector. Crystal Bio Solutions, a wholly owned subsidiary of Crystal Pharmatech Inc., is a premier provider of Biologics CMC Analytical and Bioanalytical and Biomarker services with state-of-the-art laboratories in New Jersey, California, and Marland. Crystal Bio Solutions is committed to being your trusted partner from discovery to commercialization, providing the highest quality deliverables through sound science and operational excellence. The expertise spans various therapeutic modalities including antibodies, bi/multi-specifics, proteins, ADC, CGT, mRNA, LNP, nucleotides, vaccines, and virus.
68 Chunpu Road, Bldg.3, 1st Floor, Industrial Park, Suzhou, China China/Jiangsu Province/Suzhou City, 215123 ChinaEstablished in 2010, Crystal Pharmatech is a specialized CRO/CDMO, excelling in crystal form and formulation services. Our exceptional track record includes supporting 1,000 clients and collaborating on over 2,000 compounds, showcasing our expertise in solid-state research, crystallization, pre-formulation, formulation development, and manufacturing. With a global presence encompassing three strategically located R&D centers in Suzhou (China), New Jersey (USA), and Toronto (Canada), we are powered by a skilled team of around 250 professionals. As a leader in both conventional and enabling formulation technologies, including amorphous solid dispersion, we take pride in our cGMP facilities, strictly adhering to the rigorous standards set by the FDA, EMA, and NMPA. Our integrated service encompasses the entire new drug development journey, from developability assessment and solid form screening to pre-formulation, formulation development, and CTM and commercial manufacturing. Introducing our pioneering Mol2Med program, designed to expedite small molecule lead compounds or preclinical candidates into Phase I and beyond, with unparalleled efficiency and precision. This 3-step First-Time-Right approach begins at the lead optimization/PCC stage: Step 1: Developability Assessment to guide API form selection and formulation design. Step 2: Solid form screening/selection and Preformulation. Step 3: Formulation development and CTM manufacturing, including packaging, labeling, and shipping to the clinical site. This innovative approach guarantees a robust API form and a scalable manufacturing process, culminating in a First-Time-Right formulation for Phase I. Streamlining the transition to future clinical studies upon Phase I success, our First-Time-Right approach sets the foundation for optimized drug development and success beyond. Leveraging its small molecule expertise, material science, and analytical chemistry, Crystal Pharmatech strategically entered the Biologics sector. Crystal Bio Solutions, a wholly owned subsidiary of Crystal Pharmatech Inc., is a premier provider of Biologics CMC Analytical and Bioanalytical and Biomarker services with state-of-the-art laboratories in New Jersey, California, and Marland. Crystal Bio Solutions is committed to being your trusted partner from discovery to commercialization, providing the highest quality deliverables through sound science and operational excellence. The expertise spans various therapeutic modalities including antibodies, bi/multi-specifics, proteins, ADC, CGT, mRNA, LNP, nucleotides, vaccines, and virus.
3000 EASTPARK BOULEVARD SUITE 500B Cranbury, NJ, 08512 United StatesEstablished in 2010, Crystal Pharmatech is a specialized CRO/CDMO, excelling in crystal form and formulation services. Our exceptional track record includes supporting 1,000 clients and collaborating on over 2,000 compounds, showcasing our expertise in solid-state research, crystallization, pre-formulation, formulation development, and manufacturing. With a global presence encompassing three strategically located R&D centers in Suzhou (China), New Jersey (USA), and Toronto (Canada), we are powered by a skilled team of around 250 professionals. As a leader in both conventional and enabling formulation technologies, including amorphous solid dispersion, we take pride in our cGMP facilities, strictly adhering to the rigorous standards set by the FDA, EMA, and NMPA. Our integrated service encompasses the entire new drug development journey, from developability assessment and solid form screening to pre-formulation, formulation development, and CTM and commercial manufacturing. Introducing our pioneering Mol2Med program, designed to expedite small molecule lead compounds or preclinical candidates into Phase I and beyond, with unparalleled efficiency and precision. This 3-step First-Time-Right approach begins at the lead optimization/PCC stage: Step 1: Developability Assessment to guide API form selection and formulation design. Step 2: Solid form screening/selection and Preformulation. Step 3: Formulation development and CTM manufacturing, including packaging, labeling, and shipping to the clinical site. This innovative approach guarantees a robust API form and a scalable manufacturing process, culminating in a First-Time-Right formulation for Phase I. Streamlining the transition to future clinical studies upon Phase I success, our First-Time-Right approach sets the foundation for optimized drug development and success beyond. Leveraging its small molecule expertise, material science, and analytical chemistry, Crystal Pharmatech strategically entered the Biologics sector. Crystal Bio Solutions, a wholly owned subsidiary of Crystal Pharmatech Inc., is a premier provider of Biologics CMC Analytical and Bioanalytical and Biomarker services with state-of-the-art laboratories in New Jersey, California, and Marland. Crystal Bio Solutions is committed to being your trusted partner from discovery to commercialization, providing the highest quality deliverables through sound science and operational excellence. The expertise spans various therapeutic modalities including antibodies, bi/multi-specifics, proteins, ADC, CGT, mRNA, LNP, nucleotides, vaccines, and virus.
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