As submissions get larger and resources are thinner, it can be very difficult to manage the number of documents needed in a regulatory filing. To make matters worse, your regulatory department receives documents from many sources. Plus, the types of documents that need to be compliant range from study reports to patient data listings to case report forms. Since each file can be structured differently, it makes report-level publishing challenging. To ensure these disparate documents are regulatory compliant, you need proper navigational tools and the ability quickly and accurately manage millions of links.
No other product has been able to effectively meet these requirements, until now. GlobalSubmit LINK provides a single, easy-to-use interface that not only ensures all documents are regulatory compliant, but also helps increase your team’s efficiency. We offer two versions of LINK: a standalone version and a version combined with CROSSCHECK, our leading hyperlink and bookmark quality control tool.
CROSSCHECK with LINK allows users to edit PDF files directly. This is the first product on the market to manage millions of links across thousands of files, shaving days off your quality control process. Whether you use CROSSCHECK with LINK or the standalone version, you can guarantee the highest quality, efficiency, and accuracy with every submission.