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Region

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EUROPE
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APAC
CN | JP | KR | SG | AU

Region

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EUROPE
UK | DE | ES | FR | IT
APAC
CN | JP | KR | SG | AU
 * GAMP Solutions
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Free Demo
 * GAMP Solutions
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AMPLELOGIC EBMR


ELECTRONIC BATCH MANUFACTURING RECORD


UNLOCK EFFICIENCY IN REGULATED INDUSTRIES WITH AMPLELOGIC EBMR

Schedule a Free Demo



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?

AmpleLogic eBMR 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.

Schedule a Free Demo


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 different 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 process for increased productivity.


EXCEPTION HANDLING MODULE

Ensure accurate user data input and streamline registration by implementing
validation mechanisms. Detect and swiftly address irregularities in
manufacturing to maintain process efficiency.


ELECTRONIC SIGNATURES AND AUDIT TRAILS

Robust E-Signature and thorough Audit Trails guarantee secure, traceable records
of user actions and document approvals across all modules.


BARCODES AND QR CODES

Enables tracing of actions for rooms, equipment, material, and product. Improved
traceability with barcode technology.


NOTIFICATIONS AND ESCALATION

Automated email alerts for each stage of batch record approval. Enhanced
communication and timely responses.


PRODUCT LABEL MANAGEMENT

Manages product labeling within the system. Centralized control for product
label consistency.




INDUSTRIES WE SERVE

Industry-Specific Software for Enhanced Quality and Compliance


LIFE SCIENCES

Benefit from GMP solutions customized for life sciences, pharmaceuticals, R&D,
biotech etc.


FOOD & BEVERAGES

Enhance food and beverage manufacturing with software for efficiency and
operational agility.


MEDICAL DEVICES

Transform the medical device industry with software that enhances compliance.


CANNABIS

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


GENE THERAPY

Transform gene therapy with advanced software for precision and efficiency.


COSMETICS

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


RELATED ARTICLES


CONTINUOUS ENVIRONMENTAL MONITORING USING BMR IN PHARMACEUTICAL MANUFACTURING

Continuous monitoring of environmental conditions is paramount in the
pharmaceutical industry and various other sectors, ensuring adherence to
regulatory standards product quality. Regulatory bodies like

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CRITICAL PROCESS PARAMETERS IN PHARMACEUTICAL MANUFACTURING

In pharmaceutical manufacturing, ensuring consistent production of high-quality
products is paramount. One of the key elements in achieving this goal is the
rigorous control of

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ENHANCING REGULATORY COMPLIANCE WITH PAPERLESS BMR IN PHARMA

The pharmaceutical industry is increasingly moving towards paperless Batch
Manufacturing records (BMRs) driven by regulatory expectations and the need for
enhanced data integrity and compliance.

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FREQUENTLY ASKED QUESTIONS




HOW DOES AMPLELOGIC EBMR ENSURE DATA INTEGRITY?

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




CAN IT BE INTEGRATED WITH EXISTING SYSTEMS?

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




WHAT ROLE DOES EXCEPTION HANDLING PLAY?

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




HOW DOES THE DISPENSING MODULE OPTIMIZE MATERIAL MANAGEMENT?

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




WHAT INDUSTRIES CAN BENEFIT FROM AMPLELOGIC EBMR?

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

Contact us



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