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Best Practices for Structuring Clinical Data in Medical Device Studies

Designing data collection plans for medical device studies can be cumbersome. One of the fundamental requirements of GCP and ISO 14155:2020 is to have a statistical analysis plan, together with eCRF and ePRO specifications.

But how do you ensure that clinical data is collected in line with your study goals while taking the clinical workflow at the study sites into account? 

Join us on December 7, 15.00 CET and learn how to:

  • Streamline the data collection plan with your study outcomes and the clinical workflows
  • Design forms and questionnaires that eliminate redundancy and errors
  • Avoid common mistakes in data exporting and preparation for data analysis

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