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ChemShuttle LLC - CDMO/CMO
As a premier chemistry Contract Research Organization (CRO), we are dedicatd to providing discovery chemistry services and products for new drug research and development and other supporting services to global pharmaceutical and biotechnology companies and institutions. Founded in 2010 by medicinal chemists for chemists, ChemShuttle has always embraced new technologies and partnerships to accelerate drug discovery and deliver the small molecules that our clients require to address the unmet medical needs and help patients.
United States
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15 years of experience in synthetic chemistry, PhD & Master up to 50 employees
Logistics advantage: global customers can be delivered within 2-7 working days
Confidentiality Assured: With confidentiality clauses to ensure customer data security
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Drug Substance (CDMO/CRO)
Contact ChemShuttle LLC for Contract Services Expertise
Connect with ChemShuttle LLC, a leading pharmaceutical company from United States. They offer specialized Drug Substance (CDMO/CRO). Contact ChemShuttle LLC for free and discover if they are the perfect partner for your pharmaceutical needs.
Drug Substance (CDMO/CRO)
Drug Substance CDMOs and CROs provide essential services in the development and manufacturing of active pharmaceutical ingredients (APIs). These organizations specialize in early-stage research, process development, and GMP-compliant manufacturing of drug substances for clinical and commercial use.
Pharmaoffer's Drug Substance CDMO/CRO category includes partners with expertise in small molecules, biologics, peptides, and complex chemistry, all operating under strict regulatory compliance. These providers help companies scale from lab to market efficiently and cost-effectively.
Key Functions of Drug Substance CDMOs/CROs:
API Research and Development: Providing early-stage discovery support, custom synthesis, and process optimization to streamline the development of drug substances.
Process Scale-Up and Tech Transfer: Transitioning from bench-scale to pilot and commercial scale production with validated methods and reproducibility.
GMP Manufacturing: Delivering high-quality API batches in GMP-certified environments, adhering to FDA, EMA, and other international standards.
Analytical Services: Offering comprehensive analytical method development and validation to ensure consistent quality and regulatory compliance.
Flexible and Specialized Capabilities: From small molecule synthesis to biologic and peptide manufacturing, these partners provide specialized services tailored to product-specific needs.
Explore Leading API CDMOs and CROs
Pharmaoffer connects you with trusted CDMOs and CROs for drug substance development. Our platform enables seamless access to specialized service providers equipped to support your API lifecycle from discovery to commercialization.