The EBR Implementation Guide: Part 2 – Selecting a suitable EBR
User Requirements When you are considering a new EBR system there are a number of things to consider. Chief among
Covid lessons for pharma manufacturers and why SaaS EBR is part of the answer
Do you want remote access to your batch records? Want to be able to review and release batches from home?
Learning From The Past to Improve EBR
BatchLine’s co-founder and CEO David Margetts shares key points from the history of EBR and MES that help to guide
GMP aspects of Electronic Batch Recording – Part 3: Managing Master Data
This article is the third part of a series based on applying the new GAMP GPG Data Integrity – Manufacturing RecordsContinuing
GMP aspects of Electronic Batch Recording – Part 2: Risk Assessment for Recorded Data
This article is the second part of a series based on applying the GAMP Good Practice Guide (GPG) Data Integrity –
GMP aspects of Electronic Batch Recording – Part 1: helping to meet ALCOA+ requirements
This article is the first part of a series based on applying the ISPE GAMP GPG Data Integrity – Manufacturing
Digitising Batch Records is becoming easier for GMP Manufacturers
Problem Area Most Software Can’t Reach For a long time Batch Recording software, or Electronic Batch Records (EBR or eBR if you prefer), for