Are you getting ready for your next submission?
And interested to simplify and speed up submission content creation?
Manipulating and finalizing PDFs using desktop tools is a manual task: embedding fonts, checking hyperlinks, adding ToCs and making sure they comply with HA requirements. And repeating this for 100.000s of documents. All this manual work will only increase your time to market.
Today, it does not have to be that way. You can generate FDA, EMA, PMDA (or other HA compliant) compliant PDF renditions before compiling submissions.
Join Paul Ireland in this 30-minute webinar to discover how you can easily:
- Make sure that the PDFs created are fully compliant with the Health Authority specifications. Fully automated, without user intervention.
- Reduce the dependency on manual PDF editing tools to create compliant PDFs
- Speed up time to market by moving technical content compliance earlier in your regulatory content creation process
- Save valuable time and drastically reduce risk of non-compliance
We look forward to seeing you in the webinar on May 26th.