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Overview
CaliberBRM is a leading Electronic Batch Record (eBRM) software for pharmaceutical and life sciences industries. It delivers a compliant, paperless manufacturing workflow, minimizing manual data entry errors. While compatibility with non-Empower instruments is limited, the platform helps speed up product release times.
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Starting Price
Custom
CaliberBRM Specifications
Quality Control
Compliance Management
Document Management
Shop Floor Control
What Is CaliberBRM?
CaliberBRM is a next-generation Electronic Batch Record Management System (eBRM) that drives manufacturing excellence for Pharma 4.0. This compliant software offers advanced digitalization by providing traceable batch records, automated electronic logbooks (e-Log), and consistent in-process quality checks (IPQC). Its lightweight and flexible architecture is built to be scalable beyond traditional Manufacturing Execution System (MES) capabilities, helping regulated enterprises achieve a 100% paperless shop floor and maintain compliance with 21 CFR Part 11.
CaliberBRM Pricing
CaliberBRM Integrations
Who Is CaliberBRM For?
CaliberBRM software is ideal for a wide range of industries, including:
- Pharmaceutical manufacturing
- Life sciences
- GxP-regulated enterprises
Is CaliberBRM Right For You?
For regulated industries like pharma or biotech, CaliberBRM is ideal for replacing paper-based batch records. Its EBR, e-Log, and IPQC modules ensure 21 CFR Part 11 compliance, while review by exception reduces batch review time. This scalable, error-free platform shifts focus from manual compliance to operational efficiency, supporting manufacturing excellence.
Still doubtful if CaliberBRM software is the right fit for you? Connect with our customer support staff at (661) 384-7070 for further guidance.
CaliberBRM Features
The EBR module automates and digitizes the entire batch record life cycle, moving away from error-prone paper systems. This ensures every manufacturing step is reliably documented, traceable, and easily retrievable, which is essential for maintaining strict compliance with regulations like 21 CFR Part 11 and avoiding FDA warning letters.
CaliberBRM's e-Log eliminates the risks of misplaced paper logbooks and illegible handwritten entries. It provides a secure, compliant, real-time platform to capture, track, and maintain all batch manufacturing logs, ensuring complete audit readiness and streamlined documentation across the shop floor.
Gain complete control over product quality by implementing consistent, automated, and digitalized in-process quality controls. IPQC monitors manufacturing efficiency at every critical stage, streamlines processes, and provides timely alerts for discrepancies, ensuring continuous adherence to all quality-specific manufacturing requirements and specifications.
This exclusive module within CaliberBRM provides dedicated oversight for the lifecycle of punches and dies. It automates inventory management, inspection scheduling, and discard rules. By establishing SOPs and triggering alerts for replacement, this feature ensures tool head efficacy and prevents manufacturing issues linked to equipment wear.
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