Automate Protocol And Clinical Study Reports With The Help Of Machine Learning
Regulatory Compliance
Generate protocol and CSR documents as per ICH guidelines with the help of Machine Learning.
Faster Approvals
Reduce the number of reviews required as automation generates formatted documents, reducing errors and edits by 60 - 70%.
Reduce Authoring Time
With the auto-generation of 60-70% of study and submission documents within minutes, medical writers experience tremendous time savings from authoring reports manually.
Cost Reduction
Scale down costs and improve productivity by automating study and submission document generation.
Intelligent Document Automation Enabling Faster Study Design And Regulatory Submission.
Study Setup
Speed Up your Entire Clinical Trial Process From Protocol Creation to CSR Submission.
