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Mano-Tri Pharma delivers integrated CRO and CDMO services for global partners, supported by robust internal analytical and process APIs, with strict adherence to quality systems, regulatory expectations, and ethical responsibility.
Mano-Tri Pharma is a research-driven pharmaceutical organization operating within rigorously defined scientific and regulatory frameworks. We support external clients through compliant, scalable, and data-driven development and manufacturing solutions aligned with global regulatory standards. Our focus is on building repeatable, transparent processes that ensure technical reliability, regulatory readiness, and long-term operational confidence across every engagement.
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Our organization is led by experienced scientists, engineers, and pharmaceutical professionals with domain expertise spanning development, analytical characterization, quality systems, and regulatory operations.
Senior General Manager (SGM)
Chief Scientific and Strategy Officer (CSSO)
Chief Operating Officer (COO)
Our organization is led by experienced scientists, engineers, and pharmaceutical professionals with domain expertise spanning development, analytical characterization, quality systems, and regulatory operations.
We work closely with clients to understand molecule type, development stage, regulatory goals, timelines, and risk profile, ensuring scientific and commercial alignment from day one.
A customized development strategy is designed, defining route selection, analytical approach, timelines, milestones, and deliverables with clear success criteria.
Development is executed by experienced teams under fit-for-purpose GLP/GMP like quality systems, ensuring data integrity, reproducibility, and regulatory readiness.
Results are reviewed against predefined targets. Processes and methods are optimized for yield, purity, scalability, and cost efficiency.
Complete data packages, reports, and materials are delivered, followed by a project review and recommendations for next-phase development or scale-up.
Our GLP/GMP-certified analytical spaces are outfitted with advanced instrumentation.
Our GLP/GMP-certified analytical spaces are outfitted with advanced instrumentation.
Our GLP/GMP-certified analytical spaces are outfitted with advanced instrumentation.
Our GLP/GMP-certified analytical spaces are outfitted with advanced instrumentation.
Our GLP/GMP-certified analytical spaces are outfitted with advanced instrumentation.
Our strategic initiatives are centered on bolstering research and development capabilities for complex APIs, cultivating partnerships with leading biotech firms, and ensuring adherence to regulatory requirements to fortify our competitive edge in this specialized market.
Sustainability at Mano-Tri is integrated into process design and operational planning. We implement responsible resource utilization, environmentally conscious methodologies, and continuous improvement initiatives aligned with global compliance and environmental standards. Our approach ensures scientific advancement without compromising regulatory responsibility or environmental stewardship.
Mano-Tri’s commitment to responsibility extends beyond compliance. Our initiatives support ethical operations, healthcare accessibility, and community engagement, reinforcing our belief that long-term scientific progress must be accompanied by social accountability.
Pioneering peptide innovation through precise lead selection, in vitro analysis, and expression optimization. We ensure purity, potency, and performance across every phase , from concept to clinical scale.
Advanced biologic testing with HPLC, MS, and SEC analytics, combined with validated potency and stability assays. Every formulation is crafted to meet global standards of efficacy and consistency.
Manotri Pharma provides integrated development and manufacturing services for semi‑synthetic molecules, combining fermentation‑derived cores with advanced chemical modification.
Our end-to-end quality systems ensure integrity through every process , upstream, downstream, and scale-up. With GMP-grade validation and tech transfer, we turn complex formulations into reliable, ready-to-market products.
CHO, HEK, and yeast cell lines for biosimilars.
Optimized fed-batch and perfusion systems for scalable production.
Advanced HPLC and chromatography platforms for purity and yield.
Validated processes ensuring consistency and regulatory compliance.
GMP-certified QC labs with method validation and stability studies.
Comprehensive documentation for global regulatory submissions.
Equipped with 10L to 100L automated bioreactors and digital control systems.
Our GLP/GMP-certified analytical spaces are outfitted with advanced instrumentation.
Comprehensive cold-chain systems and secure storage environments ensure material traceability, product safety.
Pilot services support process scale-up and validation between R&D and commercial manufacturing.
Reduced time-to-IND by 6 months through parallelized analytical development and accelerated tech transfer.
Optimized fermentation and downstream steps cut downstream losses and halved purification costs.
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