Facilities

Facilities

Bridgewater, New Jersey

Kashiv BioSciences’ operates from a state-of-the-art 150,000 sq.ft. R&D and manufacturing facility with capabilities for the development of innovative platform technologies, specialty products, controlled substances (CII-V), and complex oral dosage forms. It is an FDA-registered site and complies fully with Local, State, and Federal Agencies, OSHA, DEA, EPA, and cGMP Standards.

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cGMP Manufacturing Facility

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Technicians operate a three-layer tablet press used for controlled release products

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Corporate Headquarters and oral R&D and Manufacturing Site

PISCATAWAY, New Jersey

Kashiv BioSciences’ 50,000 sq. ft. R&D facility has capabilities for mammalian cell line development, advanced analytical characterization, bioassay development, and small-scale manufacturing of complex proteins and monoclonal antibodies.

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Analytical Characterization Lab

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Cell Line Process Development

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Biosimilar R&D Facility

CHICAGO, ILlinois

Kashiv BioSciences’ 100,000 sq.ft. R&D and manufacturing facility has capabilities for development and manufacturing of commercial-scale microbial cell lines, drug substance, and a fill and finish line for prefilled syringes and vials.  It is an FDA-registered site and complies fully with Local, State, and Federal Agencies, OSHA, EPA, and cGMP Standards.

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Upstream Production Suite

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Injectable Fill and Finish Line

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Biosimilar R&D and Injectable Manufacturing Facility

AHMEDABAD, GUJARAT, INDIA

Kashiv BioSciences’ 125,000 sq.ft. R&D facility contains state-of-the-art analytical labs for characterization, stability, bioassay development, process development, and small scale manufacturing of complex proteins for biosimilars. This site also conducts R&D for prodrugs and 505(b)(2) programs.

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India office and R&D facility

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Advanced analytical suites for biosimilar, 505(b)(2), and prodrug development

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Analytical labs equipped with the latest technology