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65%
reduction in document review times
4 out of 5 top contract research organizations
75%
of the top 20 global pharmaceutical companies
4 out of 5 of the top defense contractors
Collaborate on edits, approve and finalize reviews faster
Enable document owners to optimize workflows, minimize time spent gathering contributions, consolidating feedback and recording changes. Streamline project timelines and deliver quality documents.
How will Ideagen enhance your document review process?
Reduce document review time by 65%. Accelerate your projects, secure faster approvals and get to market quicker.
Reduced review time
Cut down document review time by up to 65%, accelerating project timelines, translating to faster approvals and quicker time to market.
Full audit clarity
Detailed audit trail captured in an automatically generated report.
Automatic activity tracking
Remove manual tracking of all document changes.Advanced redaction
Color codes and categories help make redaction easy for EMA Policy 70 compliance.
Integrations and technology partners
Integration with Veeva Vault, Intelinotion and other leading quality management and control solutions.
Make external collaboration easy and secure
Work securely with external reviewers without giving them access to internal systems.
Using PleaseReview makes the formal review of documents by multiple Stakeholders easy. I particularly like how the comments are able to be added easily and clearly, and then collated, so everything is tracked in one place. Very reassuring and keeps documents well organised when working on multiple projects. The integration with the Veeva document management system is helpful as multiple logons are not required.
User in Pharmaceuticals
It is a stable tool that everyone can use to centralize reviews. We can tag specific people and create discussion threads. I always use the review report/log for comment resolution meetings and minutes and works great.
User in Pharmaceuticals
See Ideagen in action with a demo personalized to you. See how our solution addresses your specific challenges. Watch our demo video now.
Document review masterclass
Packed full of critical time-saving tips you don’t want to miss, this guide brings together all our expert-led tips on how to improve document review efficiency and quality with industry-leading best practices.
Ideagen PleaseReview customer stories
Loved by highly regulated industries, Ideagen PleaseReview has been adopted by closely monitored sectors due to the software offering businesses an easy way to ensure documents comply with industry standards and regulations.
Additional reading
Why speed now determines who wins contracts in regulated manufacturing
Document quality during proposal development creates competitive advantage. Control the complete document lifecycle, from collaborative drafting through approval to archive.
Read more
Why clinical trial success rates are declining and what document collaboration has to do with it
Document quality during trial development creates risks that QMS alone can't prevent. Control the document lifecycle, from first draft to final archive.
Read more
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.
Read more
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.
Read more
How V2X achieved operational excellence
Discover how robust functionality and intuitive design streamlined V2X's peer review process effectively.
Read more
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.
Read moreFive productivity hacks to streamline proposal collaboration and win more business
For bid and proposal leaders in EMEA's highly regulated industries
Read moreWhy 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.
Read more
Centralized databases for regulatory compliance: A practical guide for businesses
Discover how a centralized database for regulatory compliance can enhance efficiency mitigate risks and support global operations.
Read more
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.
Read moreTake action
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