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KBI Biopharma, Inc. vs Scinai Immunotherapeutics Ltd.

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CategoryKBI Biopharma, Inc.Scinai Immunotherapeutics Ltd.
Listed sitecdmoboth
SummaryGlobal CDMO offering cell line development, process and analytical development, formulation development, and clinical and commercial manufacturing for mammalian and microbial biologics.Boutique biologics CDMO providing analytical method development, process development, and cGMP manufacturing for biotech clients from early research through Phase 3, backed by over 20 years of experience and state-of-the-art facilities.
Services
  • Cell-Line Development
  • Process Development
  • CMC Analytical Development
  • Formulation Development
  • Recombinant Protein Manufacturing
  • Microbial Fermentation
  • Upstream Processing
  • Downstream Processing
  • Quality Control Testing
  • Stability Testing & Storage
  • Monoclonal Antibody (mAb) Manufacturing
  • Biologics Development & Manufacturing
  • CMC Regulatory Submission Support
  • CMC Analytical Development
  • Process Development
  • CMC Regulatory Submission Support
  • Technology Transfer
  • Recombinant Protein Manufacturing
  • Biologics Development & Manufacturing
Modalities
  • Biologics (Monoclonal Antibodies)
  • Biologics (Other)
  • Biologics (Monoclonal Antibodies)
Indications
  • Dermatology
  • Dermatology
  • Immunology
  • Rare Disease
Locations
  • Durham, Durham, North Carolina, United States
  • Research Triangle Park, Research Triangle Park, North Carolina, United States
  • Boulder, Boulder, Colorado, United States
  • Louisville, Louisville, Colorado, United States
  • The Woodlands, The Woodlands, Texas, United States
  • Geneva, Geneva, Geneva, Switzerland
  • Leuven, Leuven, Flemish Brabant, Belgium
  • Patriot Park, Patriot Park, NC, United States
  • Hamlin Road, Hamlin Road, NC, United States
  • Hamlin Road, Durham, North Carolina, United States
  • Cell Line Development Center of Excellence, Geneva, Switzerland
  • Headquarters, Jerusalem, Israel
  • Yavne CDMO Facility, Yavne, Israel
Certifications
  • FDA · Identifier: cGMP
  • EMA · Identifier: European QP (EMA) audit passed
  • Israeli Ministry of Health · Identifier: Israeli MoH audit passed for Phase 3 clinical trial production
ReviewsReview summary appears after site-level review signal gate opens.Review summary appears after site-level review signal gate opens.