Cleaning ValidationMade Simple
Calculate Maximum Allowable Carryover (MACO) limits with industrial precision. Trusted by pharmaceutical leaders worldwide.
500+
Pharma Sites
100%
Audit Ready
99.9%
Precision
TRUSTED BY LEADING PHARMACEUTICAL COMPANIES WORLDWIDE
Features
Everything You Need for Cleaning Validation
Comprehensive tools designed specifically for pharmaceutical manufacturing. From calculation to documentation, we have got you covered.
How It Works
From Input to Validation in Minutes
Our streamlined workflow takes you from data entry to audit-ready documentation in four simple steps.
Input Your Data
Enter product details, equipment specifications, and select your preferred calculation method. Our smart forms guide you through each field.
- Product A and B parameters
- Equipment surface area
- Batch sizes and daily doses
Calculate MACO
Our engine instantly calculates MACO limits using your chosen methodology, applying PDE, Dose-based, or 10 ppm criteria automatically.
- PDE-based calculation (ICH Q3D)
- Dose-based criteria mapping
- 10 ppm limit application
Risk Assessment
Automated risk assessment performed as per given inputs, identifying critical cleaning parameters and equipment bottlenecks.
- Automated Risk Assessment
- Process input analysis
- Compliance risk scoring
Reports & AiDMS
Generate auditable MACO reports and manage them via our AI-based Document Management System (AiDMS) with 21 CFR compliance.
- Auditable MACO Reports
- AiDMS Integration
- Complimentary PDE Reports
Why IntegriQ
Transform Your Cleaning Validation Process
Join hundreds of pharmaceutical companies who have modernized their cleaning validation workflows. Our platform delivers measurable improvements in efficiency, accuracy, and compliance.
Save 90% Time
Automate tedious calculations and report generation. What took hours now takes minutes.
Reduce Compliance Risk
Built-in regulatory checks ensure your validations meet FDA, EMA, and WHO standards every time.
Improve Accuracy
Eliminate manual calculation errors with validated algorithms and automatic unit conversions.
Complimentary PDE Data
Get realtime online PDE reports as a complimentary subscription with your license—industry leading toxicology data.
21 CFR Part 11 Ready
Full regulatory compliance for electronic records and signatures. Auditable and secure by design.
Cost-Effective
One-time license at ₹49,999 with no recurring monthly fees. Predictable 3-year cycles.
Proven Results
Based on feedback from 500+ pharmaceutical companies using IntegriQ across India & Global
Pricing Plans
Strategic Partnership Plans
Scalable cleaning validation compliance solutions designed for modern pharmaceutical excellence.
+ Implementation & Validation
Implementation
₹1,09,000
Validation
₹49,999
Total First Year Investment
₹3,27,999 + GST
Core Features Included:
- Advanced MACO Calculation Engine (PDE / 100 ppm / Dose-based Methods)
- End-to-End Online PDE Report Onboarding & Controlled Workflow Management
- Integrated API Database for Toxicological & Regulatory Data Access
- Advanced Equipment Surface Area Calculator with Schematic Equipment Design Report Generation
- Automated Risk Assessment Report with Structured Compliance Documentation
~ ₹1,33,000 effective yearly
Implementation
₹81,750
Validation
₹49,999
Total 3-Year Investment
₹5,30,749 + GST
Exclusive 3-Year Benefits:
- Reduced Implementation Cost (Save ₹27,250)
- Priority 24/7 Regulatory & Tech Support
- Locked Pricing: No Annual Hikes for 3 Years
Experience IntegriQ Risk-Free
Empower your HODs and Validation team with a 14-day full-feature enterprise trial.No commitment required.
Payment Terms & Policy
50% Advance upon confirmation
50% Before Go-Live
GST applicable as per norms
Client retains full ownership of data
Renewal required after license period
All prices are in Indian Rupees (INR). GST (18%) will be added to the final invoice.
Our partnership framework is designed to provide long-term regulatory assurance and technical stability for global pharmaceutical manufacturing.
Professional Report Templates
Generate audit-ready documentation in seconds. Our templates are designed to meet the most stringent global regulatory requirements.
Template
Auditable MACO Report
Comprehensive MACO calculation report with full traceability of PDE, Dose, and 10 ppm criteria.
- Calculation Methodology
- Equipment Matrix
- Regulatory Citations
- Electronic Signatures
Template
Validation Risk Assessment
Automated risk assessment report as per given inputs, highlighting critical cleaning parameters.
- Worst-case Analysis
- Matrix Approach
- Solubility Data
- Equipment Complexity
100% Audit Compliance Guaranteed
All generated reports follow FDA, EMA & WHO structural guidelines.
Documentation
Comprehensive Resources for Every User
From quick start guides to advanced API documentation, we provide everything you need to get the most out of IntegriQ.
// Calculate MACO using PDE method
const result = await macopro.calculate({
method: "PDE",
productA: {
name: "Ibuprofen",
pde: 10.0, // μg/day
batchSize: 500 // kg
},
productB: {
minDailyDose: 100 // mg/day
},
equipment: {
surfaceArea: 25000 // cm²
}
});
console.log(result.maco); // 2.5 mgPro tip: Use our SDK for JavaScript, Python, and R to integrate MACO calculations directly into your existing workflows.
Built with Guidance from Industry Experts
IntegriQ was developed with invaluable insights and mentorship from these distinguished pharmaceutical professionals who shaped our vision and validated our approach.
We extend our heartfelt gratitude to these visionary leaders whose expertise, guidance, and unwavering support made IntegriQ possible. Their dedication to advancing pharmaceutical quality standards continues to inspire our mission.
FAQ
Frequently Asked Questions
Everything you need to know about IntegriQ partnership models and compliance features. Cannot find the answer you are looking for? Contact our team.
Ready to Simplify Your Cleaning Validation?
Get your IntegriQ license today and join 500+ pharmaceutical companies who trust our solution for their cleaning validation needs.
Email Us
sales@integriq.cv
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Visit Us
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Audit Pass Rate
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