GAMP-Compliant AI Platform for Life Sciences & Regulated Industries
  • Low-code aPaaS
  • Careers
  • Low-code aPaaS
  • Careers

AmpleLogic eBMR

Electronic Batch Manufacturing Record | eBMR Software in Pharma

Unlock Efficiency in Regulated Industries with AmpleLogic eBMR

Trusted by 100+ Pharma Companies Globally

Centralized Electronic Batch Record Management

Digitize and centralize batch manufacturing records, process parameters, material usage, and in-process checks within a single EBMR platform to ensure real-time visibility, accuracy, and operational control.

Accurate, Compliant, and Audit-Ready Records

Ensure standardized batch templates, controlled data entry, electronic signatures, and complete audit trails to maintain data integrity and comply with global regulations such as FDA 21 CFR Part 11, GMP, and ALCOA+ principles.

Seamless Cross-Functional Collaboration

Enable production, quality assurance, quality control, and regulatory teams to securely access, review, and approve batch records in real time, improving efficiency and reducing review cycle times.

Secure, Controlled Audit Access

Provide role-based, read-only access for auditors and inspectors with full traceability, version history, and instant retrieval of batch documentation to support faster regulatory inspections.

Revolutionizing Pharmaceutical Manufacturing

AmpleLogic eBMR stands out with its modular design and low code platform, offering tailored solutions for pharmaceutical and biotechnology industries. With features like real-time integration, dispensing modules, and electronic signatures, it ensures compliance with global regulatory standards.

Feature Section

Customizable Modular Design

Tailor processes for each batch effortlessly.

Seamless Integration

Real-time visibility with ERP, LIMS, and other systems.

Exception Handling

Detect and resolve irregularities with precision.

Authentication & Traceability

Active Directory integration, biometrics, and barcodes for enhanced security.

Why choose AmpleLogic eBMR Solution?

AmpleLogic eBMR Solution boosts productivity by automating quality checks, cutting compliance costs, and streamlining batch reviews. Its electronic records prevent errors, ensuring precise decision-making. The software speeds up product changes, meets regulatory standards, and improves efficiency in pharmaceutical manufacturing.

Features of AmpleLogic eBMR

Modular Design

Tailor processes with a drag-and-drop interface for each batch. Effortlessly manage specific activities for individual batches.

Integration Capabilities

Real-time visibility and traceability with ERP, LIMS, and other MES control systems. Seamless coordination across departments for improved efficiency.

Dispensing Module

Specify raw materials and weight-age calculations. Optimize material management with precise dispensing.

Packing Components

Manage scenarios involving bi-layer and co-packing. Efficiently handle diverse packing requirements.

Electronic Batch Records Module

Facilitates routing, reviewing, and approval of manufacturing records. Streamlined batch review processes improve productivity.

Exception Handling Module

Ensures accurate user data input and streamlined registration using built-in validation mechanisms. Detects and addresses irregularities swiftly to maintain process efficiency.

Electronic Signatures and Audit Trails

Robust e-signatures and thorough audit trails ensure secure, traceable records of user actions and document approvals across all modules.

Barcodes and QR Codes

Enables tracking of actions for rooms, equipment, materials, and products. Improves traceability through barcode and QR code technology.

Notifications and Escalation

Automated email alerts at each stage of batch record approval ensure enhanced communication and timely responses.

Product Label Management

Manage product labeling within the system with centralized control to ensure consistency and compliance.

Streamline Manufacturing with eBMR

Transform your batch record processes with AmpleLogic eBMR — modular, compliant, and built for pharmaceutical excellence.

Request a Demo

Industries We Serve

Industry-Specific Software for Enhanced Quality and Compliance

FAQ’s

Get Answers to All Your Queries

Through electronic signatures, audit trails, and a structured batch records system.

Yes, it seamlessly integrates with ERP, LIMS, and other MES control systems.

It detects and resolves irregularities in manufacturing processes, ensuring smooth operations.

It allows specifying raw materials and weight-age calculations for precise dispensing.

Apart from pharmaceuticals, it caters to biologics, medical devices, CDMOs, chemical, generics, and more.