In Clinical Trials, Medical Writing requires high volume of content to be reviewed from a variety of sources to prepare Clinical Study Reports.
Safety narratives is a key section of the Clinical Study Reports and requires review of data on each subject from different sources to prepare summaries. ICH guidelines stipulate a no. of details to be included in these narratives.
Current manual approaches can be very time and effort intensive.
Our solutions help you automate the reading of content from different forms and preparation of draft summaries of safety narratives and other Medical Writing tasks.
