TRUCHEMY EBMR
Digital Batch Production Record | eBMR Solution for Pharma
Enhance Productivity in Regulated Sectors with Truchemy’s eBMR Platform
A digital solution that automates batch documentation, enhances compliance, reduces manual errors, and streamlines pharmaceutical manufacturing processes.
Transforming Pharmaceutical Production
Truchemy eBMR distinguishes itself through its modular architecture and low-code platform, delivering customized solutions for the pharmaceutical and biotech sectors. Equipped with capabilities like real-time system integration, dispensing functionalities, and digital signatures, it supports adherence to international regulatory requirements.
Flexible Modular Architecture
Easily adapt workflows to fit each batch’s specific needs.
Smooth System Connectivity
Live data exchange with ERP, LIMS, and other platforms.
Anomaly Management
Identify and address deviations accurately.
Verification & Tracking
Boosted security through Active Directory, biometric access, and barcode scanning.
Why Opt for Truchemy eBMR?
Truchemy eBMR significantly enhances operational efficiency in pharmaceutical manufacturing by transforming traditional paper-based processes into streamlined digital workflows. By automating and digitizing quality inspections, the system ensures real-time data accuracy and traceability, which reduces manual errors and facilitates faster issue resolution. It also helps cut down on regulatory compliance costs through built-in validation protocols and audit-ready documentation.
With simplified and automated batch record reviews, Truchemy eBMR shortens production cycle times and boosts productivity across departments. Its robust electronic record-keeping ensures precision in data capture, enabling informed and timely decision-making. The platform also supports swift implementation of product changes, ensuring agility in response to market or regulatory updates.
Fully aligned with global regulatory standards like FDA 21 CFR Part 11 and EU Annex 11, Truchemy eBMR provides a secure, compliant environment for pharmaceutical operations. Additionally, it empowers teams with insightful analytics, user-friendly dashboards, and customizable workflows, ultimately leading to improved product quality, reduced waste, and operational excellence.”
Flexible Architecture
Customize workflows using an intuitive drag-and-drop interface. Seamlessly handle batch-specific tasks with ease.
Connectivity Features
Live data access and end-to-end traceability with ERP, LIMS, and other MES systems. Smooth interdepartmental collaboration for enhanced operational efficiency.
Material Dispensing Unit
Define input materials and calculate weight distribution. Enhance material handling through accurate dosing.
Packaging Module
Handle bi-layer configurations and co-pack scenarios. Streamline operations for varied packaging needs.
eBatch Records System
Enables workflow management, record review, and approval in manufacturing. Enhances batch verification efficiency to boost productivity.
Error Control Module
Validate user inputs and simplify registration with robust verification checks. Quickly identify and resolve process deviations to uphold manufacturing efficiency.
Digital Sign-Offs and Activity Logs
Secure e-signatures and comprehensive audit trails ensure traceable, tamper-proof records of user actions and approval workflows across all modules.
Encoded Identification System
Supports end-to-end tracking of facilities, assets, and inventory using barcode and QR technologies for improved traceability.
Alerts and Escalation
Automated email notifications at every step of the batch record approval process. Improved communication and prompt action.
Labeling Control System
Handles and standardizes product labels within the system, ensuring uniformity and centralized control.