- Biologics Development & Manufacturing
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Biologics Development & Manufacturing Excellence
At Mano-Tri Pharma, we are redefining biologics innovation through advanced GMP pharmaceutical manufacturing and biologics development services. With decades of scientific expertise, we empower biopharma partners to transform complex molecular ideas into market-ready therapeutics, efficiently, safely, and at global standards of quality.
Comprehensive Expertise Across the Biologics Spectrum
Core Capabilities:
- Cell Line Development & Characterization – Stable, high-yield expression systems for complex biologics.
- Upstream & Downstream Process Development – Scalable and reproducible manufacturing pipelines.
- Formulation & Analytical Method Development – Robust assays and validated analytical support.
- Viral Clearance & Sterile Fill-Finish – Ensuring safety and sterility at every stage.
- End-to-End GMP Pharmaceutical Manufacturing – From pilot to commercial batch production
- Globally compliant facilities approved by FDA, MHRA, and other leading agencies.
- Over 140 biologics projects successfully delivered across multiple modalities.
- More than 25 INDs enabled through strategic scientific partnerships.
- Proven efficiency with industry-leading titres and reduced development timelines.
Advanced Manufacturing Infrastructure
Our state-of-the-art manufacturing facilities are designed for high-volume, flexible production of biologics and nucleic acid-based therapeutics.
Capabilities Include:
- Mammalian Expression Systems – For high-quality, post-translationally modified proteins and antibodies.
- Microbial Expression Systems – For high-yield recombinant protein production.
- pDNA & mRNA Manufacturing – Precision-driven synthesis and purification for transformative therapies.
- Single-Use Bioreactors (50L–2KL) for rapid scalability.
- High-Speed Vial Filling Lines – Up to 1 million vials/day for both clinical and commercial supply.
- Why Partner With Us
Seamless integration of Molecular Biology Services and bioanalytical laboratory services.
Expertise in custom peptide synthesis services and oligonucleotides synthesis for advanced biologics.
Commitment to sustainability, compliance, and scientific excellence.
Frequently Asked Quesions
Mano-Tri Pharma provides GMP Pharmaceutical Manufacturing in FDA and MHRA-compliant facilities, including single-use bioreactors (50L-2KL), high-speed vial filling lines, and proven upstream/downstream processes. Our integrated workflows, which span from cell line generation to fill-finish, ensure that biologics production is consistent, scalable, and regulatory-ready.
Yes. We offer comprehensive Analytical Method Development Services, which include assay development, method qualification, virus clearance validation support, and formulation analytics. These competencies are critical for biopharma partners working in biologics and biosimilar manufacturing, including the Top Biosimilar Companies in India.
Absolutely. Our infrastructure supports mammalian cell culture systems for antibodies and complex proteins, as well as microbial systems for recombinant proteins. This covers experience in Microbial Fermentation Manufacturing, Microbial Fermentation Services, and high-yield microbial procedures utilized to produce Microbial Fermentation Products.
Absolutely. Our infrastructure enables mammalian cell culture systems for antibodies and complicated proteins, as well as microbial systems for recombinant proteins. This covers experience in Microbial Fermentation Manufacturing, Microbial Fermentation Services, and high-yield microbial procedures utilized to produce Microbial Fermentation Products.
Yes. Mano-Tri Pharma provides Peptide Synthesis Service, Solid Phase Peptide Synthesis, Oligonucleotides Synthesis, and Custom Oligonucleotide Synthesis for pDNA, mRNA, and hybrid constructs used in modern biologics. These capabilities complement our core manufacturing strengths, enabling rapid development of complex modalities beyond traditional protein therapeutics.
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