How to automate PDF submission content preparation to speed up publishing (including a practical demo)
Are you spending valuable time on manually manipulating PDFs for compliance?
Adding bookmarks to PDFs where there are none; checking & adding internal hyperlinks; running PDFs through OCR tools, adding table of contents, checking PDF properties for accurate navigation, PDF version, and all the other PDF requirements to make your PDFs compliant.
And doing all these using various desktop tools and plugins, right before the publishing stage?
What if automation prepared PDFs for compliance in seconds; making this a task you actually did not have to think twice about?
Think about it. You receive a PDF that contains no bookmarks, no table of contents, and no hyperlinks. Within a few moments, this PDF becomes fully compliant with the US FDA requirements and is ready to be included in a submission.
Today, this is possible thanks to automation. And we would love to show you how.
Join one of our sessions on November 9, Thursday and discover how PDF compliance for submissions can be much easier, faster, and involving less manual work.
You will not only hear what is possible; but also see what automation can do in a practical demonstration during the session.
Looking forward to seeing you in our session!
* Please make sure to register with your company email address!
Learning Objectives
See how you can easily leverage automation to:
Save valuable time in manual PDF editing for compliance:
Reduce the need for desktop PDF editing tools/plugins
Improve the way you work with the PDFs you internally create, or you receive from external stakeholders
Streamline manual-intensive PDF preparation process for one or more health authorities
Generate HA compliant PDFs in seconds, with little to no manual work involved.
We look forward to seeing you in one of our sessions on November 9, Thursday.
Who should attend?
Regulatory Affairs and Operations
Regulatory Information Management
Submissions and Global Submissions
Management/Project Management
Medical, Technical, and Regulatory Writers
Clinical Data/Data Managers
Information Technology and Support Personnel
Document and Records Management/Specialists
Essential Document Process and Business System Owners
Regulatory Standards Implementation Specialists and Associates
Clinical Operations and Processes
Quality Management
Quality Assurance/Quality Control and Compliance Professionals
Strategic Planning and Operations
Contract Research and Service Support Providers
Emerging Pharmaceutical/Biotech/Device Professionals