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latest news : ‘Control’ emerges as the critical competitive advantage for 2026, new report reveals

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AS 9100 AS9102 AS 9145 AS 13100 ISO 9001 ISO 10002 ISO 13485 ISO 14001 ISO 15189 ISO 17025 ISO 27001 ISO 45001 ISQM 1 Global Internal Audit Standards™ FedRAMP

latest news : ‘Control’ emerges as the critical competitive advantage for 2026, new report reveals

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Architecture, engineering & construction Aerospace & defense Audit, accounting and advisory Aviation Education Energy & Utilities Financial Services Food & beverage Government Healthcare Laboratories Life sciences Manufacturing Pharmaceuticals

latest news : ‘Control’ emerges as the critical competitive advantage for 2026, new report reveals

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latest news : ‘Control’ emerges as the critical competitive advantage for 2026, new report reveals

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latest news : ‘Control’ emerges as the critical competitive advantage for 2026, new report reveals

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latest news : ‘Control’ emerges as the critical competitive advantage for 2026, new report reveals

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latest news : ‘Control’ emerges as the critical competitive advantage for 2026, new report reveals

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latest news : ‘Control’ emerges as the critical competitive advantage for 2026, new report reveals

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latest news : ‘Control’ emerges as the critical competitive advantage for 2026, new report reveals

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latest news : ‘Control’ emerges as the critical competitive advantage for 2026, new report reveals

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latest news : ‘Control’ emerges as the critical competitive advantage for 2026, new report reveals

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    65%

    reduction in document review times

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    4 out of 5 top contract research organizations

    75%

    of the top 20 global pharmaceutical companies

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    4 out of 5 of the top defense contractors

    Intro

    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.

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    Delivering life changing therapies & products, faster

    Technical writers across life sciences, aerospace, defense and legal contracts streamline their document review process with Ideagen

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    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

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    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. 

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    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.

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    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.

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    Additional reading

    /bynder-asset/bynder:1B2EA5FA-AA70-4230-A9474BFD6824440E/Landscape_MD/SINGLE-IMAGE_aircraft-engineers-laptop_feb25.jpg?1749636442000

    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.

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    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.

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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.

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    Five productivity hacks to streamline proposal collaboration and win more business

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

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    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.

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    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.

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    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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    We’ll work closely with you to understand what success looks like for your team – and you’ll see how Ideagen Internal Audit can help you achieve it. 

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