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Case 04/Engineering Compliance/EPC / Manufacturing / Pharma

DrawEX — P&ID Compliance Scoring

Validates P&ID drawings against 35+ compliance checkpoints in under three minutes instead of four hours.

ClientEPC services leader with 20+ years in pharmaceutical plant design
The challenge

What was breaking

Each P&ID drawing required a manual review against 35+ compliance checkpoints — equipment labelling, line numbering, flow direction, control loops and instrument placement — costing engineers 4–5 hours per drawing and creating review backlogs across multi-disciplinary teams.

  • 4–5 hours of expert effort per drawing
  • 20–30% interpretation variance between reviewers
  • Review cycles slowing project delivery schedules
The solution

DrawEX

Built on GEN8, DrawEX combines computer vision, document understanding and semantic rules to parse drawings, score compliance and generate a review-ready report in roughly three minutes.

  • CV-based parsing of equipment, lines and annotations
  • Semantic rule engine for 35+ compliance parameters
  • Component-level pass / partial / fail scoring
  • Critical-issue identification and prioritisation
  • Branded, audit-ready report templates
Solution design

How it works

5 stages
  1. 01

    Upload

    P&ID drawings ingested as PDF or CAD via the DrawEX interface.

  2. 02

    Parse

    AI identifies equipment, instrumentation, process lines and annotations.

  3. 03

    Evaluate

    Extracted data is scored against 35+ predefined compliance parameters.

  4. 04

    Score

    Pass / Partial / Fail status with parameter-level notes and component references.

  5. 05

    Report

    Standardised, review-ready report delivered in ~3 minutes, 4 clicks.

Business impact

Before vs. after

MetricBeforeAfterImprovement
Validation time per drawing4–5 hours<3 minutes99% faster
Manual QA labour100% manual<5% oversight95% automation
Interpretation variance20–30% rework<2% rework90% reduction
Large project review2–3 weeks2–3 days90% faster
ScalabilityHeadcount-limited1,000+ drawings/dayUnlimited
Key outcomes

What changed

  • 99% time reduction in drawing validation
  • Uniform compliance interpretation across evaluations
  • Team growth without proportional resource increase
  • Regulatory and GMP alignment with consistent, traceable reports
  • Easily extendable to new compliance frameworks
Capabilities

Inside the build

CV-based parsing of equipment, lines and annotations
Semantic rule engine for 35+ compliance parameters
Component-level pass / partial / fail scoring
Critical-issue identification and prioritisation
Branded, audit-ready report templates
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We adapt these blueprints to your domain, data and governance constraints — typically delivering a working prototype in weeks.

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