4 Ways CMMS Makes Life Sciences Regulatory Compliance Easy
Maintaining compliance amid tens of thousands of regulatory standards can be a major challenge for companies in the life sciences sector, which remains among [...]
Maintaining compliance amid tens of thousands of regulatory standards can be a major challenge for companies in the life sciences sector, which remains among [...]
Maintaining accurate manufacturing data is critical to improving plant performance and demonstrating regulatory compliance. In the United States, the Food and Drug Administration (FDA) requires [...]
Maintenance professionals play a critical role in driving Good Manufacturing Practice (GMP) compliance for organizations in the life sciences. A validated computerized maintenance management system [...]
Medical device manufacturers are required to follow Good Manufacturing Practice (GMP) procedures to ensure that their products are safe, reliable, and effective. The US Food [...]
Tracking and documenting Good Manufacturing Practice (GMP) compliance can feel like a heavy lift. That’s why most life sciences organizations use digital tools like a [...]
For pharmaceutical manufacturers, adhering to Good Manufacturing Practices (GMP) is the most effective way to deliver safe, pure, and effective products to consumers. However, compliance [...]
What Is Emergency Maintenance? Emergency maintenance is urgent repair work required when equipment unexpectedly fails and poses an immediate risk to safety or operations. [...]
Three types of maintenance software dominate the asset management software market: computerized maintenance management system (CMMS) software, enterprise asset management (EAM) software, and asset [...]
What is Maintenance Planning? Maintenance planning is the process of determining what maintenance work needs to be done and how it should be carried [...]
Learn the difference between DFMEA and PFMEA and when you should use each. Identifying the failure modes of processes, designs, and assets is a [...]