Are you struggling to produce PDFs that meet the requirements of different regulatory agencies around the world? Do you find yourself spending hours, or even days, manually editing PDFs to meet the FDA, EMA, PMDA, etc. requirements?
Today, this process does not have to be this complex and difficult.
Join us in this webinar + practical demo, and see how you can reduce manual work and risks and introduce automation to help accelerate time to market. We will talk about saving time, and avoiding common pitfalls when preparing PDF documents for submissions.
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
Paul Ireland will also walk you through a 15 minute practical demonstration on how all this can be achieved. Fully automated.
We look forward to seeing you in our webinar on January 13th, Friday.
