Medical Device Software 62304 Compliance
February 22, 2019 - Online Event ON CAWebinar Compliance
info@webinarcompliance.com
Phone:4169154458
The webinar will leave you with the information needed to create and maintain good documentation that meets FDA compliance standards. You will learn about what must be done and what must not be done. In addition, you’ll learn about the various computer system validation deliverables and how to document them. This session will provide insight into the IEC 62304 standard as it is applied to medical device software. You will learn about industry best practices for the delivery of reliable and safe software for medical devices. This webinar is intended for those working in the FDA-regulated industries, including pharmaceutical, medical device, biological, animal health and tobacco. Functions that are applicable include research and development, manufacturing, Quality Control, distribution, clinical testing and management, adverse events management and post-marketing surveillance.