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  • IAS Pharma2024
    Day 3
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    Andrew Lawton

    Consultant at Risk Based Approach

    SPEAKER: Day 2
    GCP TRAINING: Impact Of Ich E8 R1 On Clinical Trials/Clinical Development

    Expertise
    RBA (25yr), RBM (11yr), ICH E6 / E8(10yr), QTL’s (11yr), Quality Management (5yr), Statistics (40+yr), Modelling (40+yr), Data Management (40+yr), Fraud and Misconduct detection (37yr), Medical/Clinical Research (42yr), Regulatory bodies (10yr), Endpoint Adjudication(19yr)

    Companies
    NHS, Boehringer Ingelheim, TransCelerate, Consultancy(next slide)

    Education
    BA Hons Maths/Geology, Research (PhD) Statistical Geophysics
    40+ publications, 2 most recent won DIA author of the year with TransCelerate papers SDV as a quality measure and Central Monitoring

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    The IAS PHARMA 2025 is organized by Xcene Research, an African Contract Research Organization committed to providing clinical trials access to a more diverse population in Africa.

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