We just recently completed a webinar on the automated Quality Management System this week, and while there were a few minor hiccups, we can call it a success in our book. One of the things that struck me was we had four speakers in the webinar, all from different regions of the world. Yet we were able to collaborate fairly seamlessly - four organizations working in tandem to tell our attendees about Quality Management Software .
eMDR, electronic medical device reporting, is an efficient method of submitting vigilance reports to the Center for Devices and Radiological Health (CDRH) at the FDA.
A white paper by Patrick Kenny of Microtest Laboratories.
Best Practices that Enable Life Science Companies to Mitigate Risk and Increase Audit Productivity
eMDR: Why Start Now, and How your QMS will Help
How to Filter Corrective Actions: Not Everything Needs to be a CAPA!
Automated Audit Management: Best Practices that Enable Life Science Companies to Mitigate Risk and Increase Audit Productivity
This TechTip will provide a step-by-step overview of a gamma irradiation validation process that complies with the standards
OVERVIEW OF AN ETHYLENE OXIDE VALIDATION
SmartPDR™ is a 100% web‐based solution that goes beyond device tracking by providing a complete lifecycle management and relationship of devices, patients, physicians and hospital data to help manufacturers understand overall product utilization and performance to improve marketing and sales effectiveness while&...