Showing 1 - 7 results of 7 for search 'Rick A. Vreman', query time: 0.05s Refine Results
  1. 1
    Getting the Right Evidence After Drug Approval

    Getting the Right Evidence After Drug Approval by Rick A. Vreman, Rick A. Vreman, Hubert G. M. Leufkens, Aaron S. Kesselheim

    Published 2020
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  2. 2
    Real World Data in Health Technology Assessment of Complex Health Technologies

    Real World Data in Health Technology Assessment of Complex Health Technologies by Milou A. Hogervorst, Milou A. Hogervorst, Johan Pontén, Rick A. Vreman, Rick A. Vreman, Aukje K. Mantel-Teeuwisse, Wim G. Goettsch, Wim G. Goettsch

    Published 2022
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  3. 3
    Regulatory reliance pathways during health emergencies: enabling timely authorizations for COVID-19 vaccines in Latin America

    Regulatory reliance pathways during health emergencies: enabling timely authorizations for COVID-19 vaccines in Latin America by Ivar T. van der Zee, Rick A. Vreman, Lawrence Liberti, Mario Alanis Garza

    Published 2022
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  4. 4
    Bridging the gap: Can International Consortium of Health Outcomes Measurement standard sets align outcomes accepted for regulatory and health technology assessment decision‐making of oncology medicines

    Bridging the gap: Can International Consortium of Health Outcomes Measurement standard sets align outcomes accepted for regulatory and health technology assessment decision‐making... by Rachel R. J. Kalf, Rick A. Vreman, Diana M.J. Delnoij, Marcel L. Bouvy, Wim G. Goettsch

    Published 2021
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  5. 5
    Synergy between health technology assessments and clinical guidelines for multiple sclerosis

    Synergy between health technology assessments and clinical guidelines for multiple sclerosis by Milou A. Hogervorst, Rick A. Vreman, Anna Zawada, Magdalena Zielińska, Dalia M. Dawoud, Brigit A. deJong, Aukje K. Mantel‐Teeuwisse, Wim G. Goettsch

    Published 2023
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  6. 6
    The Role of Regulator-Imposed Post-Approval Studies in Health Technology Assessments for Conditionally Approved Drugs

    The Role of Regulator-Imposed Post-Approval Studies in Health Technology Assessments for Conditionally Approved Drugs by Rick A. Vreman, Lourens T. Bloem, Stijn van Oirschot, Jarno Hoekman, Menno E. van der Elst, Hubert GM Leufkens, Olaf H. Klungel, Wim G. Goettsch, Aukje K. Mantel-Teeuwisse

    Published 2022
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  7. 7
    Associations between uncertainties identified by the European Medicines Agency and national decision making on reimbursement by HTA agencies

    Associations between uncertainties identified by the European Medicines Agency and national decision making on reimbursement by HTA agencies by Lourens T. Bloem, Rick A. Vreman, Niels W. L. Peeters, Jarno Hoekman, Menno E. van derElst, Hubert G. M. Leufkens, Olaf H. Klungel, Wim G. Goettsch, Aukje K. Mantel‐Teeuwisse

    Published 2021
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