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Co-authoring and document review software

Escape the email chaos of document review with our co-authoring and document review software. 

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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.

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. 

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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. 

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Automated workflow

All comments and suggested changes are captured in the system, facilitating easy to follow discussion threads. Eliminate the admin of email trails for good. 

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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. 

 

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Reconciliation reports

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.

 

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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. 

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