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European Biopharmaceutical Review

eCOA Technology in Vaccine Clinical Trials

Immunisation is one of the most successful and cost-effective public health interventions, protecting individuals against several serious, preventable, and sometimes, deadly contagious diseases, with a common example being the measles, mumps, and rubella vaccine. As essential as they are for preventative healthcare, vaccines are facing challenges in clinical trials and the industry is responsible for moving them faster through the process.

Vaccine developments face similar challenges to other therapeutic areas such as processing large volumes of manual data, which can be costly, time-consuming, and inefficient. Additionally, vaccine clinical trials often have aggressive timelines, and sponsors require a cost-effective and robust solution for data collection. By integrating electronic clinical outcome assessment (eCOA) with existing technologies, researchers can reduce the burden for study teams, increase patient compliance and retention, and improve overall study outcomes – quickly. Making the switch from traditional paperbased processes to an eCOA solution in a vaccine trial can offer many tangible benefits.

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Katie Garner is the Therapeutic Areas Advisor at CRF Bracket. 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.
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