Our Paperless eBMR/eBPR software enables pharmaceutical manufacturers to replace manual batch records with compliant, real-time electronic documentation. Designed to meet GMP, WHO-GMP, USFDA, and EU-GMP regulations, the system ensures full traceability, minimizes human error, and maximizes production efficiency.
Enhance compliance, reduce errors, and accelerate batch release with our eBMR/eBPR automation.
Real-Time Batch Tracking
Electronic Signatures & Audit Trail
Configurable BMR/BPR Templates
In-Process Checks & Validation
Error-Free Batch Closure & Review
21 CFR Part 11 & Annex 11 Compliant
Role-Based Access Controls
Deviation & Change Control Integration
Integrated Master Formula Management
Seamless QC/QA Connectivity