Standards events May 2012 (3)

This webinar on alarms in patient monitoring devices will show how you can address FDA concerns regarding alarm standards and safety. You will understand use, misuse, and the way users react or not react to alarms and how you can design new devices and re-design current products using robust human engineering principles. Why Should You Attend: FDA is seeking to reduce “alarm fatigue"...

ISO 13485:2003 is a quality management system standard specially written for the medical device industry and is on the U S Food & Drug Administration (FDA) list of recognized consensus standards. ISO 13485 is also a critical system to assist with compliance to Canadian Medical Device regulations, European Medical Device (MDD) and IVD Directives, Japanese PAL requirements, and many other...

As we move forward into the next millennium, the real challenge for many enterprises will be navigating the complexities of an increasingly globalized marketplace. Furthermore, with the declining effectiveness of traditional advertising channels, companies will now have to globalize the operations in one way or another. The industry has seen an increasing trend of companies partnering with...