Regulatory Requirements for Software Validation – March 19-21, 2018 in Arlington, VA
This 3-day course focuses on the requirements contained in the Quality System regulation specific to software validation. The course explores the latitude and flexibility of the FDA's expectations and provides conceptual ways to meet compliance [...]
Webinar: Writing Human Factors Plans and Reports – March 15, 2018
As a medical technology developer who seeks to apply human factors engineering (HFE) effectively to produce safe and effective devices and to satisfy regulators' requirements and expectations, you may be frustrated that pre-existing guidance only [...]
Integrating Risk Management into the Quality System Course – March 12-14, 2018 in Arlington, VA
This comprehensive 2.5 day course for medical device manufacturers presents risk management concepts used throughout the quality system as well as the life cycle of the product, from design…to manufacturing…through post-production. For more information: http://www.aami.org/events/eventdetail.aspx?ItemNumber=5626
International Conference on Medical Device Standards and Regulations – Arlington, VA – March 22-23, 2018
The International Conference on Medical Device Standards and Regulations will bring together regulators and standards leaders from around the world to report on some of the latest developments in this arena and discuss how medical [...]