Co-authoring and document review software
Escape the email chaos of document review with our co-authoring and document review software.
Revolutionise your document review process
Document review is crucial to compliance, but the process is often a challenge. Our document review tool gives you more control from start to finish. It cuts down the time, effort and cost of document collaboration, so you can focus on quality.
Turn documents around faster
Don’t waste time searching for documents, juggling formats and multiple reviews.
Improve document quality and control
All edits can be tracked and traced so nothing slips through the net.
Collaborate securely with external parties
Keep all your stakeholders engaged at every stage of the project.
Less travel, fewer meetings
Be more productive wherever you are with instant online collaboration.
"We have been able to almost eliminate the amount of time authors spend collating comments into the next version and are now far more efficient about resolution of conflicting reviewer comments."
Manager Regulatory Affairs
Pearl Therapeutics, Inc.
Real-time collaborative environment
The whole document review process is managed from a single and secure online space. Contributors can work together in real-time without creating conflicting versions.
Review documents in original format
Navigate between different types of documents with ease. Work in Word, Excel, PowerPoint, PDF, Images and more to ensure each type of document benefits from the same level of collaboration.
Control access and visibility
Manage access for each document and split this up into sections so that contributors can only see the content they are required for to ensure sensitive information is kept confidential.
All actions and comments that take place on a document are captured and recorded, which is detailed in the comprehensive reconciliation report. Providing you with a detailed audit trail ready for regulators.
Putting together an IND application for the FDA?
Download our checklist to ensure a smooth and successful application. It also includes advice on how to arrange a pre-IND meeting with the FDA.