We aspire to work on products and processes that are complex and hazardous. Our diverse and vast 'Organic Chemistry' experience in the field of synthesizing and characterizing Reference Standards like Drug Impurities, Metabolites, Gluconarites, Secondary API standards and Stable Isotope Labelled compounds has caused a need for taking much higher responsibilities of solving problems !
As a prominent Contract Development & Manufacturing Organization (CDMO), Clearsynth offers a powerful network of companies that provide comprehensive, end-to-end solutions for preclinical and clinical outsourcing services. We specialize in both Drug Substance / API and Drug Product development for Biologics and Small Molecules, helping (bio)pharmaceutical companies swiftly progress from the research phase to the clinical stages. At Clearsynth CDMO, we pride ourselves on delivering integrated services that compress timelines to market, accelerating the drug development process. With facilities strategically located across North America, Europe, and India, we are well-equipped to support your drug development initiatives on a global scale. Our medium-sized CDMO ensures personalized dedication to each client's projects, while our extensive expertise in preclinical and clinical drug development and manufacturing ensures that your project is in capable hands.
At Clearsynth CDMO, we combine scientific expertise in both Small Molecules and Biologics with a strong foundation in scale-up knowledge and a flexible mindset. Our dedicated team of experts is committed to focusing on your success, providing tailored solutions to meet your specific needs. Whether you require CDMO manufacturing services for novel Small Molecule therapies or intricate Biologics, we possess the capabilities and experience to address the unique challenges of each project. Our comprehensive approach ensures seamless integration of services, from early-stage development to full-scale manufacturing. By partnering with Clearsynth CDMO, you gain access to a dynamic team that is responsive to your requirements, driven by innovation, and dedicated to delivering exceptional results.
At Clearsynth CDMO, we are more than just a CDMO company; we are your strategic partner in achieving pharmaceutical excellence. Our unwavering commitment to your success is rooted in our dedication to understanding your project's unique needs and tailoring our services accordingly. As we collaborate on your drug development journey, you can count on us to navigate the intricacies of preclinical and clinical outsourcing services with precision and efficiency. With a strong global presence and an unyielding focus on quality, we are well-positioned to drive your project from concept to reality. Let's work together to bring your groundbreaking therapies to life.
Our State of Art R&D centre at Hyderabad is well equipped with 150+ Research scientists.
The sophisticated analytical lab houses- LCMS, GCMS, TGA, Prep. HPLC, UPLC, NMRs, ELSD, PDA & RI Detectors and Chiral separation columns that enable our scientists to develop and transform any process at a record breaking speed of 10-14 weeks..Ready for tech transfer !
Illuminating Biomolecular Insights through Specialized NMR Services
Cultivating Excellence in Contract Drug Manufacturing Solutions
Clarity and Precision through Expert Analytical Services
Elevating Possibilities through Small Molecule Precision
Forging Future Solutions through Advanced Process Development
Navigating Innovation Pathways with Contract R&D Excellence
Illuminating Biomolecular Insights through Specialized NMR Services
Cultivating Excellence in Contract Drug Manufacturing Solutions
Clarity and Precision through Expert Analytical Services
Elevating Possibilities through Small Molecule Precision
Forging Future Solutions through Advanced Process Development
Navigating Innovation Pathways with Contract R&D Excellence