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    VintaBio

    CDMO
    United States
    https://www.vintabio.com/

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    Advanced Modalities
    Analytical & Bioanalytical Services
    Chemistry, Manufacturing and Controls
    Company Overview

    About

    VintaBio is a pharmaceutical CDMO offering comprehensive services.

    Key Expertise

    Specialized in Quality Control, Stability Testing, Method Development

    Therapeutic Areas

    Immunology
    Rheumatology
    Quick Facts
    HQ:United States
    Founded:2001
    Employees:1,991
    Capabilities & Services

    Core Capabilities

    • Peptide Synthesis
    • Small Molecule API
    • Formulation Development

    Types of Organization

    GMP Manufacturing
    Quality Systems
    Regulatory Support

    Dosage Forms

    Inhalation

    Containment Capabilities

    BSL-2 (Biosafety Level 2)

    Production Scales

    Phase III Clinical Trials
    Commercial Scale
    Clinical

    Markets Served

    Europe
    Regulatory Approvals
    Drug Approval HXYUK9
    FDA · #APR-WCTOZA2M · 2020-09-01
    Drug Approval SRKUUF
    EMA · #APR-2WE2B4AR · 2019-05-01
    Certifications

    FDA Registration

    U.S. Food and Drug Administration
    Cert #: CERT-KCRFOWDM
    Issued: 2020-06-27
    Expires: 2025-03-22

    EMA GMP Certificate

    European Medicines Agency
    Cert #: CERT-W1RDJPDM
    Issued: 2020-02-25
    Expires: 2025-10-24

    WHO GMP

    World Health Organization
    Cert #: CERT-Q7ASJL31
    Issued: 2020-12-18
    Expires: 2025-10-15
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    Key facts about VintaBio

    • VintaBio is headquartered in the United States.
    • VintaBio was founded in 2001.
    • VintaBio has 1,991 employees.
    • VintaBio's capabilities include Peptide Synthesis, Small Molecule API and Formulation Development.

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    CDMOs in United StatesCDMOs in North AmericaSmall Molecule API CDMOsFormulation Development CDMOsInhalation CDMOsBSL-2 (Biosafety Level 2) CDMOs
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