How to automatically check & fix Word & PDF documents for compliance
Regulatory submissions are one of the most critical milestones for Life Sciences organizations. Submitting on time & in full compliance with regulatory agencies' requirements, remains a challenge.
Submissions can consist of thousands of documents. These are authored, reviewed, updated & formatted in tools like MS Word to strict guidelines before inclusion in dossiers.
Ensuring section numbering is sequential, web links aren’t included, headings are used appropriately, tables are formatted correctly, approved fonts are used, hyperlinks have targets & are colored correctly in MS Word documents. Checking bookmarks & hyperlinks have the correct zoom level, initial page view is as expected, file is optimized & doesn’t exceed size limits in PDF content. Organizations spend a huge amount of time ensuring that these & other aspects of their content are in order prior to submission.
Save your spot in 2 simple clicks for our 30-minute webinar on September 26th.
What will you walk away with?
After following this 30-minute session, you will be able to:
Understand that many of your authoring checks and fixes can be fully automated with emerging technology.
Understand that automating the validation of PDF files against Health Authority guidelines is possible much earlier in the process, and can save time and reduce the risk of non-compliance
Walk away with practical tips on how rendering technology can help streamline regulatory submission processes
Get a clear understanding of the additional benefits of fully automated processes provide over batch processing.
Save your spot in 2 simple clicks for our 30-minute webinar on September 26th.
PS: You have already other plans for September 26th? No problem, registering will give you access to the recording and other valuable post-webinar material.