Life science & pharmaceuticals

Take control of your co-authoring, review and redaction process when working on complex documents, including IND and FDA applications.

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Find out more about how our software can help within the life sciences and pharmaceuticals industry.
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The biggest benefit of Ideagen PleaseReview is the time we have saved when it comes to manually reviewing a document

Thomas Class, Head of Regulatory Affairs - Translate Bio

Manage all aspects of complex clinical documents

When launching new products into the market, whether it be medical devices, vaccines or disease management products, companies often need to produce an extensive number of complex documentations, and possibly in several different languages. Our software supports all document creation throughout the clinical research and trial phases.

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Save time, meet deadlines and evidence accountability

Our collaboration tools help life science and pharmaceutical companies streamline and reduce the review cycle by 65%. Collaborate in real-time and remove the manual effort of collating comments and edits. Set granular levels of permissions, resolve conflicting comments, and show accountability through the comprehensive audit trail.

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Case study

Translate Bio use Ideagen PleaseReview to collaborate seamlessly with regulatory authorities around the world

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Case study

Ideagen’s PleaseReview helps Lexicon Pharmaceuticals save hundreds of hours by reducing document review times

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Customers using our solution

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Discover our collaboration resources for life sciences

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The essential guidebook to better medical writing

Discover how to collaborate successfully on document reviews.

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75% of the world’s top pharmaceutical companies use Ideagen PleaseReview

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Ideagen PleaseReview’s ROI value

See how Ideagen PleaseReview can help you accelerate your time to market.

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Pre IND meeting FDA: your need-to-knows

A guide to pre IND meetings with the FDA.

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