Best Electronic Batch Records (EBR) Software for GitHub
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Compare the Top Electronic Batch Records (EBR) Software that integrates with GitHub as of September 2026
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This a list of Electronic Batch Records (EBR) software that integrates with GitHub. Use the filters on the left to add additional filters for products that have integrations with GitHub. View the products that work with GitHub in the table below.
What is Electronic Batch Records (EBR) Software for GitHub?
Electronic batch records (EBR) software is a software system used to manage and organize batch production data. It allows for the creation, tracking, and modification of electronic records for each step involved in the production process. The software can be used in various industries such as pharmaceuticals, food processing, and consumer goods manufacturing. EBR software provides real-time monitoring capabilities, ensuring accuracy and consistency in record-keeping. It also offers customizable features to meet the specific needs of different production environments. Compare and read user reviews of the best Electronic Batch Records (EBR) software for GitHub currently available using the table below. This list is updated regularly.
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1
Qualio
Qualio
Qualio is the leading quality and compliance platform built exclusively for emerging life sciences companies. MedTech, pharma, biotech, and diagnostics teams use Qualio to standardize quality processes, connect them to regulatory obligations, and gain real-time visibility into compliance health. With a modern eQMS at the core and Compliance Intelligence layered on top, Qualio helps teams get audit ready in weeks and stay audit ready forever — without spreadsheets, fire drills, or heavyweight GRC systems. What Qualio delivers: ✔️ Audit ready in weeks ✔️ Inspection ready anytime — no fire drills ✔️ Faster market entry ✔️ Lower total cost of compliance ✔️ Confident, risk-managed scaling -
2
Greenlight Guru
Greenlight Guru
Trusted by over 1,000 medical device manufacturers, Greenlight Guru is a quality management system built for the medtech industry. The platform is architected around regulatory reality, not generic enterprise frameworks. FDA 21 CFR Part 820/QMSR, ISO 13485, ISO 14971, EU MDR, and 21 CFR Part 11 are aligned at the foundation, not added later. Implementation takes weeks, not quarters. With 80+ audit-tested templates and medtech-expert support, you skip the separate validation project and go live faster. Greenlight Guru integrates AI-powered automation to reduce manual work while maintaining the audit trail and documentation rigor your business requires. With 15 years in medical device QMS, Greenlight Guru helps you pass inspections, accelerate time-to-market, and sustain commercial success.
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