February 6-8, 2018Anaheim Convention CenterAnaheim, CA
2018 Event Content Schedule
Use the scheduling tool below to browse all the available sessions, speakers and topics at this year's event. Find the content and sessions to fit all of your educational needs and ensure you get the most out of your time at the show.
How do you know the appropriate quality standards for outsourcing analytical projects to support medical device product development? Should you require a GLP or GMP regulated laboratory? What does an ISO 17025 certified analytical laboratory mean? Your Quality Assurance department may dictate multiple tiers of quality requirements. However, certain requirements may limit the types of analysis performed, or even result in lengthy investigations on investigational results. This presentation compares and contrasts the different quality standards from FDA, OCED and ISO, to help you understand how these quality standards apply to analytical testing for medical device development.