eBMR for Pharma
Electronic Batch Manufacturing Records for Pharmaceutical Manufacturing
Complete Digitization Platform | 21 CFR Part 11 Compliant | FDA-Validated
Why Electronic Batch Manufacturing Records?
Transform paper-based processes into efficient, compliant digital workflows
The Paper Problem
Many pharmaceutical manufacturers still capture batch manufacturing details on paper—a cumbersome process involving:
- Manual printing of process parametric data from each manufacturing step
- Walking across the manufacturing floor to collect paper printouts
- Manual compilation and verification by QA individuals
- Risk of errors, delays, and compliance issues
Complete eBMR Solution
Everything you need in one integrated platform—no separate packages or hidden costs
All-Inclusive Platform
Unlike vendors who sell modules separately, Atachi NGIMES includes everything in one license—no hidden costs.
- Recipe/Master Batch Record Management
- Weighing & Dispensing
- Batch Execution
- QA Review & Approval
Seamless IoT Integration
Connect to any PLC from any vendor—legacy or modern—without expensive HMI/SCADA upgrades.
- Pull data from wide variety of PLCs
- Real-time process parameter display
- Remote parameter control
- Equipment on/off switching
Lifetime Data Retention
We handle data retention throughout product life—no upgrades, no migrations, no worries.
- Complete batch history access
- No platform upgrade worries
- Continuous improvement insights
- Beyond retention compliance
Starting Your eBMR Journey
Common concerns and how Atachi NGIMES addresses them
Challenge: Legacy Equipment
Process data comes from PLCs of different vendors and models spanning 20-30 years. How do you integrate them without replacing everything?
Atachi Solution:
NGIMES-IIoT seamlessly pulls data from any PLC—no additional HMI/SCADA investments needed. We work with your existing automation layers while ensuring 21 CFR Part 11 compliance.
Challenge: Hidden Costs
Many vendors sell Recipe Management, Weighing & Dispensing, Training Management, and other features as separate packages. Costs add up quickly.
Atachi Solution:
Everything is included in one platform, one license. Recipe Management, Weighing & Dispensing, Training Management, QMS, Deviations, CAPA—all bundled together.
Challenge: Compliance Without Breaking the Bank
Do you need to make every machine 21 CFR Part 11 compliant before implementing eBMR? That's expensive and time-consuming.
Atachi Solution:
NGIMES provides compliance at the system level. You don't need to retrofit every machine. Implement eBMR with flexibility and compliance at every step.
Beyond eBMR: The Complete Platform
eBMR is just the beginning. What happens when you need more?
Deviations & CAPA
Built-in deviation management and CAPA workflows—no separate QMS to buy
eLogBooks
Equipment logs, environmental monitoring, and cleanings—all digital
OEE Analytics
Real-time production performance, availability, and quality metrics
Training Management
Video and document training with automated certification enforcement
Mobile Support
Run on mobile devices for warehouse scanning and shop floor operations
SAP Integration
Native integration with SAP ERP and S/4HANA—built on SAP HANA technology
One Platform. One License. Complete Digitization.
No meaningless integration budgets. No juggling multiple vendors. Everything works together seamlessly.
Real Results
By leveraging Atachi NGIMES OEE for Pharma functionality, we uncovered a hidden factory of 10 percent production capacity.
Ready to Start Your eBMR Journey?
Discover how Atachi NGIMES can transform your pharmaceutical manufacturing with a complete, compliant eBMR solution.
Or call us: +1 (408) 839-1743