Validation of Manufacturing Execution Systems

Overview:

Manufacturing execution systems (MES) are increasingly commonplace in pharmaceutical manufacturing environments and they can be interfaced with many types of systems, equipment and instruments. Controlling the manufacture of pharmaceutical and medical products is critical to ensuring product quality and patient safety. This article discusses current topics, considerations and controls necessary for the validation and ongoing compliance activities required for MES. Are you using MES to ensure manufacturing excellence, improve cost effectiveness and increase ROI? CBI's 8th Annual Forum on Manufacturing Execution Systems, August 13-14 in Philadelphia features ways to improve lean manufacturing, MES deployment & integration. Attend the only event to focus on MES for the Bio/Pharmaceutical industry. Download agenda and find out what your MES data is telling you.

Manufacturing execution systems (MES) are increasingly commonplace in pharmaceutical manufacturing environments and they can be interfaced with many types of systems, equipment and instruments. Controlling the manufacture of pharmaceutical and medical products is critical to ensuring product quality and patient safety. This article discusses current topics, considerations and controls necessary for the validation and ongoing compliance activities required for MES.

 

Are you using MES to ensure manufacturing excellence, improve cost effectiveness and increase ROI? CBI's 8th Annual Forum on Manufacturing Execution Systems, August 13-14 in Philadelphia features ways to improve lean manufacturing, MES deployment & integration. Attend the only event to focus on MES for the Bio/Pharmaceutical industry. Download agenda and find out what your MES data is telling you.