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    Company profile for JANSSEN BIOTECH

    NEW Drugs in Dev: 6
    LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.

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    Sharp is a leader in commercial packaging, clinical services, and sterile manufacturing.

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    pharmacompass-1-m-2026-04-20

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    As a CDMO, Mikart offers integrated CDMO services for Solid Dose & Non-sterile Liquid formulations.

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    Trusted Global CDMO Partner Delivering End-to-End Pharma Manufacturing & Development Solutions.

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    pharmacompass-2-m-2026-04-20

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    NEWS #PharmaBuzz

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    Janssen’s Icotyde Receives Approval in US
    Janssen’s Icotyde Receives Approval in US

    17 Mar 2026

    // FDA

    https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=220149

    FDA
    17 Mar 2026
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    Janssen’s Biologics Rybrevant Fasproi Receives Approval in US
    Janssen’s Biologics Rybrevant Fasproi Receives Approval in US

    13 Feb 2026

    // FDA

    https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=761484

    FDA
    13 Feb 2026
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    Janssen’s Biologics Rybrevant Faspro Receives Approval in US
    Janssen’s Biologics Rybrevant Faspro Receives Approval in US

    13 Feb 2026

    // FDA

    https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=761484

    FDA
    13 Feb 2026
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    Janssen’s Korean facility cited for GMP violations
    Janssen’s Korean facility cited for GMP violations

    24 Sep 2025

    // RAPS

    https://www.raps.org/news-and-articles/news-articles/2025/9/janssen-s-korean-facility-cited-for-gmp-violations

    RAPS
    24 Sep 2025
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    Janssen`s Biologics Rybrevant Receives Suppl Approval in US
    Janssen`s Biologics Rybrevant Receives Suppl Approval in US

    03 Sep 2025

    // FDA

    https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=761210

    FDA
    03 Sep 2025
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    Janssen’s Biologics Tecvayli Receives Suppl Approval in US
    Janssen’s Biologics Tecvayli Receives Suppl Approval in US

    19 Aug 2025

    // FDA

    https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=761291

    FDA
    19 Aug 2025
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