BatchLine | Electronic Batch Record Solution
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Smarter, Faster, and Higher Quality Manufacturing with BatchLine..
Digital Batch Record for Pharma (eBR),
Medical Device (eDHR), & other
​GMP Regulated Products 
BatchLine

What is BatchLine?

Ground breaking cloud Electronic Batch Record (EBR) software

A ground-breaking Electronic Batch Record system, built fully on modern web technology, and designed specifically to meet requirements for GxP regulated production: pharma, biotech, cell & gene, medical device (eDHR), healthcare, supplements, herbal medicines, cannabis derived products, as well as various foods, beverages, and cosmetics. 
BatchLine entirely digitises production. From creating processes, recipes, master batch records (MBR’s), and product specifications to guiding operators engagingly through executing the process with digital work instructions, device integrations via IoT, quality review and approval of the batch electronically (review by exception), and batch record reporting and retention.   
We took the EBR concept traditionally found in large MES software and re-engineered it into a modern, simple to use and low-cost web app. Suitable for any size organization, and accessible on any device with an internet connection via our managed cloud or installed on your own infrastructure. 
BatchLine Explainer Video
Watch video with Bahasa Subtitle  |  Thai Subtitle
No big upfront costs.   All the benefits of EBR.   All the benefits of cloud.   Monthly subscription.

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Paper becomes data

Turn your paper batch record into a smart, electronic workflow; and automate formulas, lists, time calculations, and in-process-controls.

Watch 2 minutes BacthLine EBR Demo Video

​Learn how BatchLine supports compliance with GMP.

Learn more

MANUFACTURE BETTER..

FULLY COMPLIANT..

  • Remove the paper​ 
  • Review by exception
  • Manufacture Right First Time
  • ​E-Signatures with automatic date/time stamping
  • Automatic sequence control
  • See what's happening in realtime
  • Full graphical reporting
Our development team includes world-class consultants on GMP, PIC/s, GAMP, and FDA compliance with 17 years’ experience across Europe, APAC and USA.

Meets regulatory requirements of US FDA 21 CFR Part 11, EU and PIC/S GMP Annex 11.

​BatchLine is developed with quality practices and regulations at its heart, and has been qualified to the highest international standards.

All validation, qualification, SOP's, and quality documentation comes included with subscription. 



​Discuss your business requirements with one of our consultants and arrange a demo.

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+66 (0) 2630 4525           +44 (0) 1925 506 130
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