Ideagen Please Review

Transform document collaboration for regulated industries

Ideagen Please Review provides collaborative document review, co-authoring, and redaction capabilities that enable 65% faster document completion for regulated industries.

The platform supports teams from 2 to 200+ reviewers through secure real-time collaboration workflows. Built for highly regulated sectors including life sciences, aerospace, and legal contracts, it integrates with Veeva Vault and other quality management systems. The software provides comprehensive audit trails, automated change tracking, and advanced redaction capabilities for EMA Policy 70 compliance while enabling secure external collaboration.

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Additional reading

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Introduction to Ideagen Please Review

Find out how you can streamline document reviews in regulated industries and reduce review times by up to 65% with Ideagen Please Review.

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Implementing a document approval workflow with multiple approvers

Discover how a document approval workflow with multiple approvers can transform your business. Learn to automate your document review process, reduce bottlenecks and ensure compliance with an efficient and effective approval system.

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How V2X achieved operational excellence

Discover how robust functionality and intuitive design streamlined V2X's peer review process effectively.

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Pioneering cancer research meets unparalleled Veeva Vault integration

Learn how a biotech company streamlined document reviews to meet FDA, EMA and GDPR regulations while speeding up cancer therapies.

Five productivity hacks to streamline proposal collaboration and win more business

For bid and proposal leaders in EMEA's highly regulated industries

Why biotech leaders can’t afford delays in document review: The hidden risk to market access

Learn how modern document review solutions speed up clinical trials, reduce errors, and help biopharma meet regulatory deadlines in a competitive industry.

Navy Warfare Development Center cuts time reviewing critical doctrine

In naval operations, timely updates to doctrine are essential for readiness. The Navy Doctrine Library System (NDLS) faced delays and inefficiencies due to an outdated document review process. To address this, NDLS adopted Ideagen Document Review, streamlining collaboration and cutting review timelines in half.

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Four of the top five CROs select Ideagen PleaseReview to accelerate timelines

Ideagen PleaseReview has been selected by four of the top five global CROs to support the delivery of faster and more efficient clinical trials to sponsors. Find out more.

How Santa's elves use Ideagen PleaseReview to save Christmas

Discover how Santa's elves use Ideagen PleaseReview to streamline their operations and ensure a magical Christmas for children worldwide.

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5 steps to ensure a successful clinical trial

Ensure clinical trials succeed by mastering patient recruitment, utilizing smart methodologies, and harnessing real-world evidence effectively.