Paper Batch Records
Manual paper records are time-consuming, error-prone, and difficult to retrieve during audits.
Manufacturing Execution System
Electronic batch record and real-time manufacturing execution with complete compliance
TeraCliq eBMR/MES automates batch documentation, real-time data capture, equipment control, and manufacturing compliance with digitalized workflows and complete audit traceability for regulated production.
50%Reduction in batch record time
100%Digital batch documentation
30%Faster batch release cycle
ZeroTranscription errors in records
Industry Challenges
Why batch manufacturing requires digital transformation
Paper batch records, manual data entry, fragmented systems, and slow approvals create delays, errors, and weak compliance documentation that expose companies to regulatory risk.
Manual Data Collection
Operators record data manually from multiple sources, creating transcription errors and gaps.
Slow Batch Release
Collecting signatures and approvals manually delays batch release decisions and regulatory submissions.
Fragmented Quality Data
Quality checkpoints and deviations tracked separately from batch records create disconnected compliance evidence.
Weak Audit Trails
Incomplete records and manual processes make it difficult to prove compliance during regulatory inspections.
Core Capabilities
Five capability areas that power compliant manufacturing execution
Digital Batch Execution
Guide operators through recipe steps with real-time data capture, quality gates, and automated approvals.
Real-Time Data Integration
Capture in-process parameters from sensors and instruments automatically with calculated results.
Equipment Connectivity
Connect batch execution to manufacturing equipment for automated parameter logging and equipment history.
Quality Checkpoint Management
Route quality checks through approval workflow with deviation escalation and corrective action tracking.
Batch Release & Compliance
Automate batch release routing with multi-level approvals, signatures, and complete audit trail documentation.
Control Tower
Monitor manufacturing execution in real-time
The eBMR/MES provides complete visibility into batch progress, in-process performance, quality checkpoints, and release readiness, enabling managers to optimize production and ensure compliance.
- Track active batch progress and step completion status
- Monitor in-process parameters and equipment performance
- View quality checkpoint status and pending approvals
- Generate batch release documentation and regulatory reports
End-to-End Process Flow
How eBMR/MES works
A complete batch execution workflow from schedule through release, with real-time data capture and quality integration.
Batch Scheduling
Schedule batches from ERP with recipe data, materials, and expected yield parameters.
Digital Step Execution
Guide operators through batch steps with real-time data entry, equipment controls, and quality gates.
In-Process Data Capture
Capture parameters automatically from sensors and instruments with real-time calculations.
Quality Checkpoints
Route in-process quality checks through approval workflow with deviation escalation.
Batch Completion
Capture final yields, material reconciliation, and operator sign-offs at batch closure.
Batch Release & Reporting
Route release through multi-level approvals with signatures and complete batch history documentation.
Key Features
Built for pharmaceutical manufacturing, not generic MES
Digital Recipe Management
Store and execute batch recipes with step-by-step guidance and parameter tracking.
Real-Time Data Capture
Capture in-process data from multiple sources with calculated results and compliance validation.
Equipment Integration
Connect batch execution to manufacturing equipment for automated parameter logging and histories.
Quality Checkpoint Routing
Route in-process quality checks through approval workflow with deviation escalation.
Material Traceability
Track materials used in batches with lot traceability and genealogy documentation.
Batch Release Workflow
Automated release routing with multi-level approvals and electronic signatures.
Deviation Management
Capture and track deviations with impact assessment and corrective action workflows.
Electronic Signatures
21 CFR Part 11 compliant electronic signatures for batch records and approvals.
Value Delivered
Measurable benefits for manufacturing teams and quality leaders
Batch Execution
Execute batches more quickly with streamlined digital workflows and automated approvals.
Compliance
Maintain complete electronic batch records with audit trails meeting 21 CFR Part 11 requirements.
Data Quality
Eliminate manual transcription errors with real-time automated data capture.
Administrative Work
Streamline batch release approvals and documentation generation for faster throughput.
Regulatory Confidence
Provide inspectors with complete batch records and material traceability on demand.
Use Cases
Where eBMR/MES creates the most impact
High-Complexity Manufacturing
Execute complex multi-step recipes with real-time data capture and automated quality checkpoints.
Material Traceability Management
Track materials through batches with complete genealogy and finished product traceability.
Equipment Qualification Extension
Maintain equipment qualification through batch-level parameter documentation and trending.
Batch Release Acceleration
Speed release decisions with complete data packages and streamlined approvals.
Regulatory Submission Readiness
Provide regulatory agencies with complete batch records for product approvals and inspections.
Ready to digitalize your manufacturing execution?
Let TeraCliq eBMR/MES turn paper batch records into an automated, compliant, real-time manufacturing execution system.
Get Started Today