Advanced ADC Solutions…Chemistry. Conjugation. Clinical Success.
Overview
At Cohance Lifesciences, we bring together the power of precision chemistry, bioconjugation expertise, and GMP manufacturing to accelerate Antibody-Drug Conjugate (ADC) development from discovery to clinic. Our integrated approach spans innovative payload and linker development, bioconjugation strategies, and clinical-grade manufacturing — all under one agile, compliant platform.
With NJ Bio as our strategic partner, we offer a CRDMO model purpose-built for ADCs — combining deep scientific insight with end-to-end execution. Whether it’s optimizing cytotoxic payloads or scaling conjugated molecules for clinical supply, Cohance Lifesciences is your trusted partner for success in the evolving ADC landscape.
Why Cohance for Small Molecule Manufacturing?
Why Partner with Cohance for ADCs?
- Integrated CRDMO model combining chemistry, biology, and manufacturing expertise
- Global pioneers in Camptothecin (CPT) derivatives & proprietary
S-Trione technology - High-containment facilities purpose-built for high-potency payloads and conjugates
- Robust backward integration ensuring supply chain control and delivery reliability
- Regulatory-ready platforms with DMFs and Phase-appropriate GMP infrastructure
- Strategic partnership with NJ Bio for discovery, bioconjugation, and clinical execution
Manufacturing Strengths
Manufacturing Strengths
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.
Our Comprehensive ADC 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.
Route scouting, process development, and optimization
Analytical development, impurity profiling, and validation
Comprehensive process safety assessments for secure scale-up
Payload & Linker
Development
• CPT & Auristatin derivative synthesis
• Proprietary s-Trione-based payloads
• Industry-standard & custom linkers
• Containment expertise for high-potency synthesis
Integrated
CRDMO Services
• Linker-payload optimization and bioconjugation
• Phase-appropriate GMP manufacturing
• Analytical development & regulatory documentation
• Discovery to IND support, tech transfer, and scale-up
Facilities
Genome Valley R&D Center: 25,000 sq. ft. of dedicated process development and safety labs.
Commercial Manufacturing Sites: Multi-ton capacity, including facilities for HPAPIs, phosphoramidites, and other complex chemistries.
Flow Chemistry Suites: Plug flow reactors, Corning G1 systems, and photo flow platforms.
Integrated Development Services
Early Phase Development
Lab-scale feasibility, synthetic optimization, and impurity identification.
Scale-Up Readiness
Execution of engineering and validation batches using advanced reactors and process tools.
Lifecycle Services
Rework/reprocessing studies, solvent recovery, impurity fate, and purge investigations.
Special Capabilities
Expertise in hazardous reactions, air-/moisture-sensitive chemistries, stereoselective synthesis, and green catalysis.
Genome Valley R&D Center
25,000 sq. ft. of dedicated process development and safety labs.
Commercial Manufacturing Sites
Multi-ton capacity, including facilities for HPAPIs, phosphoramidites, and other complex chemistries.
Flow Chemistry Suites
Plug flow reactors, Corning G1 systems, and photo flow platforms.
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.
Genome Valley R&D Center
25,000 sq. ft. of dedicated process development and safety labs.
Commercial Manufacturing Sites
Multi-ton capacity, including facilities for HPAPIs, phosphoramidites, and other complex chemistries.
Flow Chemistry Suites
Plug flow reactors, Corning G1 systems, and photo flow platforms.
Our early-stage R&D and kilo labs are designed to support route scouting, process development, and scale-up studies.
Designed to seamlessly scale from clinical to commercial manufacturing, these facilities are compliant with global regulatory standards including the US FDA.
Genome Valley R&D Center
25,000 sq. ft. of dedicated process development and safety labs.
Commercial Manufacturing Sites
Multi-ton capacity, including facilities for HPAPIs, phosphoramidites, and other complex chemistries.
Flow Chemistry Suites
Plug flow reactors, Corning G1 systems, and photo flow platforms.
From grams to tons-trust Cohance to deliver your small molecule at scale.
Contact Manufacturing Team
Design. Develop. Deliver. Let’s bring your ADC innovation to life with end-to-end excellence.
Contact UsResources
- Webinar: Mastering Payload-Linker Chemistry for ADC Success
- Whitepaper: Innovations in Camptothecin-Based Payload Synthesis
- Case Study: Seamless Tech Transfer for a Phase 1 ADC Program
- Blog: What Makes a Reliable Payload Partner in the ADC Ecosystem?
Resource Highlights
Webinars
Navigating Regulatory Audits in Small Molecule Manufacturing
Whitepapers
Smart Scale-Up Using Flow Chemistry
Case Studies
Seamless Tech Transfer of a Multi-Step Synthesis
Blog
Building Sustainable API Supply Chains
Webinars
Navigating Regulatory Audits in Small Molecule Manufacturing
Whitepapers
Smart Scale-Up Using Flow Chemistry
Case Studies
Seamless Tech Transfer of a Multi-Step Synthesis
Blog
Building Sustainable API Supply Chains
Our Global Accreditations
At Cohance Lifesciences, every facility stands as a testament to our commitment to uncompromised quality. Below is a snapshot of regulatory approvals and certifications across our global network
API Manufacturing Facilities
API Unit I
• US FDA, EU, PMDA, Russia MOH, KFDA, COFEPRIS, CDSCO, DCA, WHO GMP
API Unit II
• EU, DCA
API Unit III
• US FDA, EDQM, PMDA, KFDA, ANVISA, COFEPRIS, CDSCO, DCA
API Unit IV
• US FDA, EU, CDSCO, DCA
API Unit V
• ISO, DCA
Formulation (FDF) Facilities
FDF Unit I
• US FDA, Health Canada, MHRA, ANVISA, COFEPRIS, Russia MOH, TGA, Philippines FDA, Tanzania FDA, Greece NOM, Uganda NDA, Germany, SFDA, CDSCO, DCA
FDF Unit II
• CDSCO, DCA
Clinical Research
CR Bio
• US FDA, DCGI, MOH Turkey, BPFK Malaysia, WHO Geneva, MHRA, GCC, NPRA Malaysia
Suven Pharma Sites
Unit 1 to Unit 4, and Unit 6
• British Safety Council, International Safety
• ISO 20400:2017, ISO 22301:2019, ISO 9001:2015, ISO 14001:2015, ISO 45001:2018, ISO 50001:2018
Unit 5
• US FDA, DCA, PPD Global Quality Compliance, EU, CDSCO
• ISO 22301:2019, ISO 9001:2015, ISO 14001:2015, ISO 45001:2018, ISO 50001:2018
Casper
• US FDA, DCA
Our ESG Aspirations
Cohance is committed to a sustainable future with ambitious goals:
- Net-Zero Emissions by 2050: Focusing on decarbonization, renewable energy, and resource efficiency, aligned with Science-Based Targets (SBTi).
- Environmental Sustainability: Enhancing green practices through sustainable procurement and biodiversity protection.
- Social Impact: Expanding community engagement in health, sanitation, and water access, while supporting economic development through CSR initiatives.
- UN SDG Alignment: Contributing to goals like Good Health and Well-Being, Clean Water and Sanitation, and Responsible Consumption and Production.
- Ethical Governance: Strengthening transparency, ethics, and responsible sourcing through global initiatives like the Pharmaceutical Supply Chain Initiative (PSCI).
At Cohance, ESG is our promise to go above and beyond, shaping a sustainable future for health science through passion, expertise, and unwavering responsibility.
History
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Experience
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Leadership Team
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ESG
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Quality & Compliance
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About usEngitech is the partner of choice for many of the world’s leading enterprises, SMEs and technology challengers. We help businesses elevate their value through custom software development, product design,
Experience
Our great team of more than 1400 software experts.
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We’ll help you test bold new ideas while sharing your.
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We deal With The Aspects Of Professional IT Services
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