Automation That Works - Life Sciences Regulatory Submission Prep Automation -Teaser

Описание: Regulatory submissions shouldn’t be a fire drill.

In this demo, see how Adlib automates the heavy lift (classifying source files, converting 300+ formats, validating PDFs, enforcing link styles/headers, and assembling submission-ready packages) so life sciences teams ship faster with fewer touchpoints and cleaner data.

What you’ll see:
• End-to-end regulatory submission prep automation demo
• Auto-classification, conversion, bookmarking, blue hyperlinks, PDF/A compliance
• Built-in validation for technical rules (blank pages, versions, sizes, link styling)
• Human-in-the-loop only where it adds value, clear error reasons and quick fixes
• Data extraction to JSON for RIM/QMS/AI pipelines (protocol IDs, PIs, narratives)
• “Bring your own LLM” with pristine, structured inputs for higher accuracy

Who it’s for:
Regulatory affairs, Clinical operations, Quality, and IT teams working with RIM/EDMS who need audit-ready, eCTD-friendly packages without night-before scrambling.

Outcomes:
Fewer reworks, faster cycle times, lower risk, and trustworthy inputs for AI and analytics.

Watch the full demo: https://www.adlibsoftware.com/events/...

Keywords: life sciences, regulatory submission automation, eCTD, RIM, EDMS, Documentum, Veeva, compliance, PDF validation, metadata extraction, AI-ready documents, HITL, GxP, SOP

#LifeSciences #RegulatorySubmissions #DocumentAutomation #eCTD #PharmaTech