Katie Garner

Katie Garner is Therapeutic Areas Advisor at CRF Health. She is responsible for providing specific therapeutic advice and supporting the therapeutic, sales, marketing and product development teams. Previously, Katie worked as a Project Manager for a Health Outcomes Consultancy and at the NHS Purchasing and Supply Agencies Centre for evidence-based purchasing. She also worked for the Medicine and Healthcare Products Regulatory Agency as a Senior Medical Device Specialist where she was responsible for the safety and regulation of in vitro diagnostic and contraceptive medical devices.

  • Poster: Can Older Users Use Electronic Clinical Outcome Assessments?

    Poster: Can Older Users Use Electronic Clinical Outcome Assessments?

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  • Utilizing Technology to Benefit Diabetes Clinical Trials - Pharmiweb

    Utilizing Technology to Benefit Diabetes Clinical Trials - Pharmiweb

    For participants in diabetes clinical trials with complex healthcare routines to manage, tech can significantly improve the patient experience. Patients can digitally report meals, blo

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  • Optimising Outcomes - eCOA in Oncology Trials

    Optimising Outcomes - eCOA in Oncology Trials

    The integration of ePRO and eCOA into routine cancer care can reduce the burden of data collection.

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  • Understanding the Benefits of eCOA in Oncology Clinical Trials13:18

    Understanding the Benefits of eCOA in Oncology Clinical Trials

    Dan Limbach of PharmaVOICE interviews CRF Health's Katie Garner, Therapeutic Areas Manager, about the benefits of using eCOA in oncology clinical trials.

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  • Best Practices for Collecting eCOA Data in Diabetes Trials 37:07

    Best Practices for Collecting eCOA Data in Diabetes Trials

    Katie Garner highlights considerations and best practices for designing eCOA solutions for diabetes clinical studies. Learn how a patient-centric eCOA system benefits both patients and investigators.

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