India's first GMP-aware AI document studio for lab & pharma professionals

Your documents.
Compliant by design.

Select your role. Choose your document. Answer 4 smart questions using anonymised placeholders. Receive a fully formatted, GMP-compliant, audit-ready document — ready to personalise and file.

"The science is yours. The paperwork is ours. Finally."

5
Verticals
50
Documents
GMP
Compliant output
0
Confidential data needed
SmartInput™
Quality scoring built-in
🔒
Your data stays safe — by design. This studio uses anonymised placeholders only. Type Product X, Batch ABC, Analyst Y — never your real data. Every [BRACKETED PLACEHOLDER] in the output is highlighted so you can find and replace before filing. Your confidential information never leaves your device.
How it works
01
Select your vertical
QC/QA, R&D, Pharma, Biotech, or Lab Management
02
Choose a document
10 world-class documents per vertical, GMP-compliant
03
SmartInput™ checks quality
AI scores your inputs for specificity, coherence and regulatory context before generating
04
Download & replace
Highlighted placeholders show exactly what to fill in before filing
✦ Exclusive Technology

Introducing SmartInput™

The only AI document studio that evaluates your inputs before generating — so you always know the quality of what you are about to receive.

01
Word Count Gating
Every question has a calibrated minimum. The Generate button stays locked until your inputs meet the threshold — by document type, by question, by role.
Layer 1 · Always active
02
Pre-Flight Quality Score
Before generating, your inputs are scored across 4 dimensions — Specificity · Coherence · Completeness · Regulatory Context — out of 100. You see exactly what is strong and what needs more detail.
Layer 2 · Score 50+ to generate
03
Dynamic Follow-Up Questions
Below score 50, SmartInput™ detects the specific gaps in your inputs and asks 2 targeted follow-up questions for your exact scenario — so your document reflects your real situation, not a generic template.
Layer 3 · Activated below score 50
✓
Thin inputs flagged before generation
✓
Specificity · Coherence · Completeness · Regulatory Context — scored individually
✓
Follow-up questions tailored to your document type and scenario
Step 1 — Select your professional vertical
Step 2 — Choose your document
Use placeholder codes throughout — Product X, Batch ABC-001, Analyst Y, Facility Z. You will replace these after downloading.
Please login & answer all questions with sufficient detail before generating.
Generated Document
⚠ Placeholder document — Replace all [BRACKETED TEXT] highlighted in yellow with your actual data before filing in your QMS or submitting to a regulatory authority.
⚗
Select a vertical to begin
Choose your professional role above to see the available documents
Complete template library — full scope of this product
50 GMP-compliant documents across 5 verticals
The complete document library for lab and pharma professionals. Documents marked ✦ Unlocked are available now. 🔒 Premium documents unlock with a subscription — sign up below to get early access.