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Av. Benjamin Franklin 19 Paterna, Valencia, 46980 SpainCurapath is a global CDMO specialized in the development and GMP manufacturing of non-viral drug delivery systems based on lipids, polymers, and advanced nanoparticle technologies. We support biotech and pharmaceutical companies from early development through commercial supply, providing tailored solutions for mRNA, DNA, gene and cell therapies, vaccines, oncology applications, medical devices, and other advanced therapeutic modalities. Our integrated end-to-end capabilities include: • Preclinical Development • Formulation Development and Optimization • Nanoparticle Design and Process Development • Process Scale-Up and Technology Transfer • GMP Manufacturing of Lipid and Polymer Excipients, Bioconjugates and Drug Substances • Analytical Method Development and Validation • Quality Control Testing and Characterization • Drug Product Manufacturing • Aseptic Fill & Finish Services for Liquid and Lyophilized Products • ICH Stability Studies • CMC Development and Regulatory Support • Commercial Manufacturing Readiness and Supply For drug substance (DS) manufacturing, Curapath offers GMP production of lipid and polymer excipients, bioconjugates, and advanced drug delivery components. Our expertise includes polymer conjugation and cross-linking technologies designed to improve drug stability, enhance bioavailability, reduce toxicity, and enable targeted delivery. We support programs from early development through scalable GMP manufacturing and commercial supply. As a full-service CDMO, Curapath provides comprehensive process development, scale-up, analytical support, technology transfer, and manufacturing solutions for advanced drug delivery programs. Our expertise spans lipid nanoparticles (LNPs), polymer nanoparticles (PNPs), targeted delivery systems, liposomes, and other next-generation formulations supporting RNA, DNA, gene therapy, cell therapy, vaccine, and oncology applications. We help clients accelerate development timelines while ensuring product quality, reproducibility, and regulatory compliance. Curapath also offers aseptic Fill & Finish services and commercial manufacturing support for clinical and commercial-stage programs. Our flexible manufacturing capabilities are particularly well suited for advanced therapies, orphan drugs, gene and cell therapy products, and other specialized applications requiring reliable GMP production, regulatory expertise, and scalable supply chain solutions. By combining development, manufacturing, analytical, and regulatory services under one organization, Curapath enables a seamless transition from preclinical development to market-ready commercialization.
One Broadway 14th Floor Cambridge, MA, 02142 United StatesCurapath is a global CDMO specialized in the development and GMP manufacturing of non-viral drug delivery systems based on lipids, polymers, and advanced nanoparticle technologies. We support biotech and pharmaceutical companies from early development through commercial supply, providing tailored solutions for mRNA, DNA, gene and cell therapies, vaccines, oncology applications, medical devices, and other advanced therapeutic modalities. Our integrated end-to-end capabilities include: • Preclinical Development • Formulation Development and Optimization • Nanoparticle Design and Process Development • Process Scale-Up and Technology Transfer • GMP Manufacturing of Lipid and Polymer Excipients, Bioconjugates and Drug Substances • Analytical Method Development and Validation • Quality Control Testing and Characterization • Drug Product Manufacturing • Aseptic Fill & Finish Services for Liquid and Lyophilized Products • ICH Stability Studies • CMC Development and Regulatory Support • Commercial Manufacturing Readiness and Supply For drug substance (DS) manufacturing, Curapath offers GMP production of lipid and polymer excipients, bioconjugates, and advanced drug delivery components. Our expertise includes polymer conjugation and cross-linking technologies designed to improve drug stability, enhance bioavailability, reduce toxicity, and enable targeted delivery. We support programs from early development through scalable GMP manufacturing and commercial supply. As a full-service CDMO, Curapath provides comprehensive process development, scale-up, analytical support, technology transfer, and manufacturing solutions for advanced drug delivery programs. Our expertise spans lipid nanoparticles (LNPs), polymer nanoparticles (PNPs), targeted delivery systems, liposomes, and other next-generation formulations supporting RNA, DNA, gene therapy, cell therapy, vaccine, and oncology applications. We help clients accelerate development timelines while ensuring product quality, reproducibility, and regulatory compliance. Curapath also offers aseptic Fill & Finish services and commercial manufacturing support for clinical and commercial-stage programs. Our flexible manufacturing capabilities are particularly well suited for advanced therapies, orphan drugs, gene and cell therapy products, and other specialized applications requiring reliable GMP production, regulatory expertise, and scalable supply chain solutions. By combining development, manufacturing, analytical, and regulatory services under one organization, Curapath enables a seamless transition from preclinical development to market-ready commercialization.
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