Pharmaceutical Documentation Platform

Your validation engineers are brilliant. Let them prove it.

ValDocs doesn't replace your QA team. It frees them from document drudgery so they can do the work you actually hired them for.

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IQ Protocol Generation

Same quality. Different timeline.

Before

6 hours

With ValDocs

11 min

Your engineer reviews & approves. The thinking stays human.

21 CFR Part 11

GAMP 5 Aligned

FDA Ready

See It In Action

Blank template to audit-ready in 2 minutes

Watch the 2-minute demo

Select Template

Your templates, your standards. IQ, OQ, PQ—whatever your QMS requires.

Generate Draft

Enter system details. ValDocs builds the protocol with proper cross-references in minutes.

Review & Export

Your engineer reviews, adds judgment, approves. Full audit trail included.

The Real Problem

You hired experts. They're buried in boilerplate.

Your best validation engineer has 12 years of experience. She's caught deviations that saved million-dollar batches. She understands your processes better than anyone.

But she spends 60% of her week copying text between templates, reformatting tables, and hunting for SOP reference numbers.

You didn't hire her to copy and paste.
You hired her to think.

ValDocs handles the assembly. She handles the judgment calls. Same rigorous output—but now she has time to catch what matters.

The Shift

Not replacement. Amplification.

What they fear

"We'll automate your docs"

Black-box systems they can't trust
Loss of control over compliance
Dependency on tech that breaks

What we deliver

"Your team, unleashed"

Full visibility into every output
Human approval on every document
Your templates, your standards

See a protocol built in 2 minutes

No pitch deck. No sales call. Just the product, working.

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