Scoop

Founded 2025

AI platform that speed up drug trials with fast, accurate regulatory filings.

Cost

Demo

Rating

★ People love it

Time to value

Quick Setup (< 1 hour)

You can use Scoop to automate the creation and maintenance of IND submissions for drug trials. It converts your study and manufacturing data into regulatory documents that stay updated as your science advances. The AI continuously reconciles changes across all sections, flags inconsistencies, and regenerates updated text when new studies complete. You get full traceability from every sentence back to source documents, making regulatory filings faster and more accurate.

What Scoop does

Upload scientific reports and CMC documentationGenerate regulatory narratives from raw dataReview flagged inconsistencies across document sectionsUpdate submissions when new study data arrivesTrack source documents for every generated sentenceExport formatted documents for regulatory filingManage version control for evolving submissionsCoordinate cross-references between document modulesAutomatically maps content to IND structureGenerates submission-ready narratives with source traceabilityFlags conflicting values across document sectionsUpdates affected sections when new studies completeDetects inconsistencies automatically during reviewsMaintains continuous versioning of regulatory documentsReads like professional regulatory writingHandles ongoing maintenance beyond initial drafts

Tutorials & Demos

Frequently asked

eCTD tools, document management systems

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