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Integrated Small Molecule Solutions – From Lab to Launch
Overview
Cohance Lifesciences delivers globally compliant, GMP-grade manufacturing solutions for small molecule APIs, advanced intermediates and starting materials. With a multi-site network of USFDA- and EMA-inspected facilities, we offer flexible production—from gram-scale validation batches to multi-ton commercial supply.
Equipped with flow chemistry, cryogenic systems, and high-pressure reactors, our plants are designed to handle complex, sensitive, and highly potent compounds with precision. Integrated analytics, backward supply chain linkages, and a commitment to continuous improvement make us a trusted partner for quality, scalability, and speed to market.
Why Cohance for Small Molecule Manufacturing?
Why Cohance for Small Molecule Manufacturing?
- Proven scale-up of niche and hazardous reactions
- Integrated analytical, safety, and engineering support
- Fully backward-integrated for supply chain assurance
- Flexible delivery formats: clinical supply, validation batches, and commercial lots
- Continuous improvement and lean practices for cost and time efficiency
Manufacturing Capabilities
Scalable
Production
Flexible volumes from gram to multi-ton capacity across multiple sites.
GMP-Ready
Infrastructure
USFDA-, EMA-, and PMDA-approved sites with validated processes and full traceability.
Technology-Enabled
Execution
Flow reactors, high-pressure systems (up to 20 kg/cm²), cryogenic capabilities (-70°C), and automation.
Regulatory
Compliance
200+ DMFs filed globally; extensive experience in audits and global market readiness.
Lifecycle
Manufacturing
Support for reprocessing, impurity purge, solvent recovery, and green manufacturing practices.
Scalable
Production
Flexible volumes from gram to multi-ton capacity across multiple sites.
GMP-Ready
Infrastructure
USFDA-, EMA-, and PMDA-approved sites with validated processes and full traceability.
Technology-Enabled
Execution
Flow reactors, high-pressure systems (up to 20 kg/cm²), cryogenic capabilities (-70°C), and automation.
Regulatory
Compliance
200+ DMFs filed globally; extensive experience in audits and global market readiness.
Lifecycle
Manufacturing
Support for reprocessing, impurity purge, solvent recovery, and green manufacturing practices.
Facilities
We operate a robust network of cutting-edge small molecule development and manufacturing facilities across India. Our infrastructure spans lab-scale discovery to large-scale commercial manufacturing — enabling faster, flexible, and scalable solutions for your drug development needs.
Our early-stage R&D and kilo labs are designed to support route scouting, process development, and scale-up studies.
CDMO R&D Unit-I, Genome Valley
Hyderabad, India
API R&D Unit-III, Nacharam
Hyderabad, India
Designed to seamlessly scale from clinical to commercial manufacturing, these facilities are compliant with global regulatory standards including the US FDA.
CDMO Unit-I, Suryapet
Hyderabad, India
CDMO Unit-II, Jeedimetla
Hyderabad, India
CDMO Unit-III, Pashamylaram
Hyderabad, India
API Unit IV, Nacharam
Hyderabad, India
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