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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The biggest benefit of Ideagen PleaseReview is the time we have saved when it comes to manually reviewing a document
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.
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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