SOLUTIONS > PROCESS

Electronic Batch Record (EBR)

Gain full visibility to easily manage your manufacturing processes

Streamline batch record management

Life sciences organizations are reaping the benefits of electronic batch records to improve efficiency, ensure accuracy, and streamline operations.

Integrate with Other Systems

Electronic batch records seamlessly connect with systems like eQMS, LIMS, and ERP to create a unified digital environment. This integration eliminates data silos, streamlines workflows, and improves coordination across production, quality, and supply chain operations. By connecting critical systems, teams gain real-time visibility and control over every stage of manufacturing.

Gain Effortless Scalability

Electronic systems adapt easily to growing production volumes and evolving process complexity. Dot Compliance supports scalability by enabling organizations to add new products, sites, or workflows without disrupting existing operations. This flexibility helps companies stay agile and maintain efficiency as they expand.

Reduce Risk of Errors

Automated data entry and recordkeeping significantly reduce human error and ensure accuracy across all production records. Built-in validation rules verify inputs at every step, maintaining data integrity and regulatory compliance. With consistent, error-free documentation, teams can trust their records and accelerate batch release.

Why Dot Compliance Electonic Batch Record Solution

Dot Compliance’s electronic batch record (EBR) solution enables organizations to monitor, manage, track, document, and report on quality processes to ensure the production of manufactured products that are compliant with global standards and regulations. This means organizations can eliminate paper trails and human error and harmonize manufacturing processes.

Features and Benefits

Gain visibility by integrating the eQMS with MES

Seamlessly integrate between eQMS and MES to deliver full visibility into EBR to easily manage manufacturing processes.

Meet compliance with regulatory agencies and standards

Ensure compliance with regulatory agencies like the FDA and the EMA, as well as cGMP standards.

Better document management

Allows users to organize, manage, and track documents, images, and other digital content necessary for conducting clinical trials.

Automate the process and alleviate the manual burden

Reduce effort associated with paper-based processes by linking quality documents in the manufacturing process, including work instructions, SOPs, electronic forms, batch records, and test results.

The eQMS that keeps you one step ahead

Dot Compliance is the industry’s first AI-powered eQMS, built to get you up and running fast – and to give you the insights to drive quality efficiently.

Smart solutions for life sciences companies at every stage

Meet the eQMS that evolves with you, from setting a foundation with core processes to the industry’s most sophisticated AI quality and compliance intelligence.