Why Implementing Manufacturing Execution Systems (MES) Improves Biopharma Quality

Batch record review is a painstaking process if your company relies on exhaustive paper records – or a combination of paper and electronic records. Today an increasing number of life sciences companies are turning to manufacturing execution systems (MES) to reduce quality issues, accelerate resolution and improve operations. With MES software, you can create a holistic electronic batch record (EBR) that not only documents the process but guides each step to minimize quality issues at the onset.

If your company is taking steps to improve documentation practices through a digital transformation, this blog may help you get started down the road of improving standard operating procedures, accelerating issue resolution, and extending gains.