GMP-Validated ERP forPharmaceuticalManufacturing
End-to-end ERP built for pharma & life sciences — from batch manufacturing and electronic batch records to GMP compliance, 21 CFR Part 11 validation, and complete supply chain traceability.
Everything Your Pharma Business Needs
Purpose-built modules for pharmaceutical and life sciences — covering every workflow from lab to launch.
Recipe & Formulation Control
Lock approved formulations and prevent unauthorized modifications through controlled version management.
- Master Recipe Locking
- Version Control
- Formulation Protection
- Controlled Change Management
- Secure Recipe Governance
A Complete Pharma ERP Suite
12 integrated modules designed specifically for pharmaceutical manufacturing — no customization needed.
Recipe Management
Master recipe locking with version control and formulation protection.
Batch Manufacturing
Electronic batch records with real-time compounding and yield monitoring.
Quality Assurance
In-process testing, stability management, and quarantine control.
Quality Control
QC testing workflows with batch release management and compliance tracking.
Regulatory Compliance
21 CFR Part 11, GMP, and GAMP alignment with CSV support.
Electronic Batch Records (eBMR)
Paperless eBMR with electronic signatures and immutable audit trails.
Supply Chain & MRP
Material requirements planning with API and excipient inventory management.
Inventory Management
Real-time inventory control with procurement and distribution tracking.
IFRS-Compliant Financials
Integrated financial management with international reporting standards.
Sales & Distribution
Order management and distribution tracking across channels.
Audit Trail Management
Immutable audit trails with complete traceability and compliance reporting.
Analytics & BI
Real-time KPI dashboards with yield, variance, and compliance analysis.
All modules are pre-validated and GxP-compliant out of the box.
Explore All ModulesCompliance-First by Design
Built specifically for pharmaceutical compliance requirements with complete digital integrity, security, traceability, and audit readiness.
21 CFR Part 11 Compliance
Full compliance with FDA electronic records and signatures requirements including secure timestamps, access controls, and validation documentation.
GMP Alignment
Built-in Good Manufacturing Practice controls ensuring pharmaceutical quality standards throughout production workflows.
GAMP Alignment
GAMP 5 Category 4 validated platform with comprehensive validation protocols and risk-based qualification approach.
Computer System Validation (CSV) Support
Complete CSV documentation including IQ/OQ/PQ protocols, validation master plans, and ongoing validation support.
Electronic Signatures
Secure electronic signature workflows with multi-level approval processes and complete audit trail integration.
Immutable Audit Trails
ALCOA+ compliant audit trails with complete traceability of all system activities and data modifications.
2-Factor Authentication
Enhanced security with multi-factor authentication ensuring authorized access to critical pharmaceutical data.
Advanced Security Protocols
Enterprise-grade security measures including encryption, role-based access control, and continuous monitoring.
Supported Compliance Frameworks
Real-Time Manufacturing Intelligence
Monitor your entire pharmaceutical operation — batch execution, quality metrics, and GMP compliance at a glance.
Active Batches
Quality Pass Rate
Pending Reviews
Deviation Alerts
Active Batch Records
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See Pharma ERP in Action
Watch how AVEEROS transforms pharmaceutical manufacturing with GMP-validated digital workflows
Trusted by Leading Pharma Companies
"AVEEROS Pharma ERP transformed our batch record management. We went from paper-based eBMRs to fully validated electronic batch records in 4 months. FDA audit preparation time dropped from 2 weeks to 3 days. The 21 CFR Part 11 compliance is impeccable."
Join Us & Learn More
Pharma ERP Webinar
GMP Validation & 21 CFR Part 11 Compliance
Pharma Manufacturing Summit
Live Demo — Booth #P-312
eBMR Implementation Workshop
Hands-On CSV Training
GMP-Validated Pricing
Pre-validated platform with 30-day free trial. No credit card required.
Billed annually · $8628/year
Billed annually · $22788/year
All plans include GMP validation docs · 30-day free trial · Cancel anytime
Need custom validation? Talk to our CSV team →
Ready to Transform Your Pharma Manufacturing?
Book a free GMP-validated demo and see how AVEEROS can streamline your pharmaceutical operations with full regulatory compliance.
What happens next:
Request a GMP Demo
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Our team will contact you within 4 business hours to schedule your personalized demo.
Pharma ERP Brochure
Complete product specifications & validation docs
Ready to Go Paperless with GMP-Validated eBMR?
Join 200+ pharmaceutical manufacturers who trust AVEEROS for GMP compliance, batch manufacturing, and regulatory reporting — fully validated and audit-ready.