Scoop

Founded 2024

Draft and update pre-clinical regulatory submissions for drug trials

Pricing model

Demo

Rating

★ People love it

Time to value

Quick Setup (< 1 hour)

You can use Scoop to draft and maintain pre-clinical regulatory submissions for clinical trials. By uploading scientific study reports and manufacturing data packages, you can automatically convert your research into structured IND filings. The system creates narrative sections with direct citations back to your source files, making reviews straightforward. It also scans your documents to flag conflicting numbers or outdated phrasing across modules. When you complete new experiments or change manufacturing processes, Scoop highlights affected sections and regenerates updated text automatically.

What Scoop does

Upload scientific study reports and manufacturing dataMap research data directly to IND regulatory modulesGenerate submission-ready draft narrativesIdentify conflicting data across filing sectionsTrace claims to specific source file sentencesUpdate document sections after new study resultsMaps uploaded scientific and CMC documents to IND submission structuresMaintains direct citation links between generated sentences and source filesDetects conflicting values and inconsistent metrics across document modulesAutomatically flags sections requiring updates after new study results arriveRegenerates regulatory narratives when manufacturing specifications changeProduces regulatory-style writing instead of generic document summaries

Pricing breakdown

Pricing model: Book a demo

Tutorials & Demos

Frequently asked

eCTD tools, document management systems, eCTD Publishing Tools, Veeva Vault (RIM/Quality), Documentum, SharePoint, Electronic Lab Notebooks (ELN)

Used by

Michael Tona

Founder / CEO @ Hubfluence

In their stack

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