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Covvalent - CDMO/CMO
We provide end-to-end molecule development and manufacturing services for small molecules, empowering customers to move from idea to commercial supply faster.
Our full-spectrum capabilities include lab-scale custom synthesis (gram quantities) and Gram to kilo-scale process development.
Commercial manufacturing under cGMP, ready for regulatory audits
Technical expertise across 30+ complex & hazardous chemistries, including: Fluorination (nucleophilic: HF/KF, electrophilic), Chiral synthesis (induction, optical resolution, enantioselective routes), Phosgenation (phosgene, diphosgene, triphosgene under strict safety protocols), Cryogenic reactions (down to –80 °C)
Process technologies offered: Stereoselective synthesis & chiral separations, High-pressure & high-vacuum operations, Bio-transformations, Continuous (flow) chemistry, Hazardous...
India
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Complex Chemistry Expertise – 30+ advanced chemistries backed by a strong R&D team
End-to-End Molecule Development from Idea to Commercial Scale
Global Quality, India Advantage – cGMP/FDA-compliant facilities, world-class SHE & IP standard at effecient pricing
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We bring deep expertise across challenging reaction classes such as
Chiral Synthesis
Fluorination
Phosgenation
Cryogenic reactions
Expertise in Phase-appropriate small molecule supplies, right from early discovery supplies to pre-clinical supplies for in vitro and animal studies, followed by process development, optimization as per target market standards, technology transfer, scale up as per phase-appropriate clinical supply requirements, till commercial manufacturing supplies.
Drug Substance (CDMO/CRO)
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Contact Covvalent for Contract Services Expertise
Connect with Covvalent, a leading pharmaceutical company from India. They offer specialized Drug Substance (CDMO/CRO). Contact Covvalent 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.