GAMP-Compliant AI Platform for Life Sciences & Regulated Industries
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AmpleLogic eBMR

Electronic Batch Manufacturing Record | eBMR Software in Pharma

Unlock Efficiency in Regulated Industries with AmpleLogic eBMR

AI-Powered APQR Software

Annual Product Quality Reviews, Reimagined with AI

Annual Product Quality Review is a critical regulatory requirement for pharmaceutical and life sciences organizations. AmpleLogic’s APQR solution enables structured, compliant, and inspection-ready reviews by consolidating quality data, automating trend analysis, and generating audit-ready reports.

Trusted by 100+ Pharma Companies Globally

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.

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.

Industries We Serve

Industry-Specific Software for Enhanced Quality and Compliance

Life Sciences

Apply Nelson Rules to detect abnormal process behaviour and statistically significant trends.

Pharmaceuticals

Enhance cannabis and tobacco manufacturing with advanced software for efficiency and flexibility.

Medical Devices

Transform the medical device industry with software that enhances compliance.

Gene & Cell Therapy

Address the complexity of advanced therapies by capturing batch-specific data, deviations.

Food & Beverages

Conduct structured product quality reviews that support safety, consistency, and regulatory expectations.

Cosmetics

Boost cosmetics and beauty operations with innovative software for process optimization.

Case Studies

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.