Automated Report Level Publishing Resource 1

Are you creating your reports manually today? Or perhaps using complex submission publishing tools to build your reports? Investigational medicinal product dossiers (IMPD), clinical study reports (CSR), annual reports, training manuals, standard operating procedures (SOP) and even full 510k & PMA submissions could all benefit from a tool designed specifically for their creation. ​Merging multiple […]

The process of preparing content for submissions is very time-consuming and financially burdensome ​Using multiple desktop tools, and spending hours or even days, manually editing PDFs to meet the FDA, EMA, PMDA, etc. requirements  ​Manually checking and fixing thousands of PDF files for submission readiness ​Re-working external content to ensure document compliance ​Validating content too late, and the risk of missing submission deadlines ​Authors

Are you using Veeva to store and manage your submission content? ​The automation of regulatory content does not need to stop there. ​Combined with the power of DocShifter, we can take automation to the next level. So you can focus on the content. ​How will this powerful combination help you save time with the following?