Driving document review efficiency in CROs
Accelerate timelines. Provide full transparency to sponsors. Deliver better quality documents.
If you work on document submissions in a CRO, this ebook sets out a simple yet game-changing solution that will transform the way you work on collaborative document reviews moving forward.
Download now to discover how others just like you have saved critical time by boosting efficiency and, ultimately, freed up more resource to focus on delivering better quality.
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Common frustrations
Lengthy email chains
Attempting to reconcile comments by email is time-consuming and the chance of missing something important is high
No control
Struggling to manage deadlines and see review progress. No clearly defined start and end points for the review cycle.
Not hitting timelines
Deadlines missed due to lengthy review process
External collaboration
Difficult to collaborate securely in the document with external partners.
No version history
Hard to keep track of changes to the document. Some reviewers' work would be overwritten and/or lost.
Admin burden
Difficult for the document owner to consolidate comments from multiple different copies of a document.
Frustrations with SharePoint
Difficult to collaborate on content-rich document reviews with high-volume teams.
Formatting issues
Issues with document formatting being maintained across versions.
32% of FDA submissions fail due to quality issues
Given that 32% of FDA submissions have critical data conformance issues, CROs need to invest more time and effort into improving the accuracy and consistency of their documents. This means they simply cannot afford to waste time on clunky and outdated workflows that can now be streamlined.
In our ebook, we give you practical and actionable tips to help you standardise your review process, boost efficiency and liberate your contributors from tiresome admin. So you can all spend more time on delivering what matters to a higher standard.
Key takeaways
- Create a disciplined process for document reviews
- Free up more time to deliver better quality documents
- Get therapies to market more efficiently
- Provide full transparency to sponsors
- Achieve inspection-readiness