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Regulatory submissions are one of the most critical milestones for Life Sciences organizations. Submitting 

 with regulatory agencies' requirements, remains a challenge. Life Sciences organizations adopt cutting-edge technology, but the 

technology alone doesn't guarantee compliance

 & that timelines are met. Efficient processes combined with technology does.  

This webinar outlines how organizations can 

streamline content preparation processes for their submission documents

Regulatory 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. Multiple groups are involved in ensuring they meet the technical requirements, so how can you make sure that:

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.

It is impossible to eliminate all manual steps but 

During our presentation on August 26th, we will explain how such a reduction in manual steps can be achieved. It is possible to fully automate many of the checks & fixes performed manually or in batch today; both on your original source Word content & on your submission-ready PDFs. 

After following this 30-minute session, you will be able to: 

Lessons Learned on Document Preparation in Life Sciences (Abstract from the DIA Regulatory Submissions, Information and Document Management Forum 2022)