The conference will focus on how to set up clinical and performance studies with medical devices and IVD. In addition, delegates will learn\u00a0 how to implement the regulation and guidelines within this field and how to appropriately collect the data needed to support the clinical and performance evaluation pathways.<\/span><\/p>\nThe programme will cover topics from all fields of early stage strategic consideration, practical examples from speakers that are working on implementing the strategy, compliance issues, and key areas such as:<\/span>
\n– Clinical document build up for various types of studies<\/span>
\n– Working with sites (contracting, compliance etc.)<\/span>
\n– EDC and data management processes and documentation<\/span>
\n– Monitoring<\/span>
\n– Risk assessment and other related collateral topics<\/span><\/p>\nWe look forward to welcoming you in London at The 3rd Conference on Clinical Studies with Medical Devices and IVDs (CSMD2024).<\/span><\/p>\nSincerely,\u00a0\u00a0<\/span><\/p>\n<\/div>\n<\/div>\n\n
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