ISO 13485 provides requirements for quality management practitioners involved in the design, production, installation and servicing of medical devices and related services
Upgrade your expertise with a deep understanding of ISO 13485 as well as how to interpret and implement it at your organization. Take on a productive role in your organization’s auditing process. This comprehensive training will help you identify non-conformance to the standard, and lead audits for your organization or beyond.
Quickly and efficiently learn the requirements of ISO 13485 and take a greater role in your organization’s quality management system. Designed for individuals who are involved with quality management systems, implementation, and auditing to the ISO 13485 series of standards for medical devices and related services.
This program provides introductory information for those organizations who are considering transitioning from the Aeronautic, Space, and Defense industry to the Food & Drug Administration (FDA), Medical Device Manufacturing market. Participants will examine the controls between the AS9100 Standard and FDA Regulations and identify similarities.
ISO 13485 not for you? Explore our range of QMS courses.
In a highly competitive industry, quality is everything.
SAE powers your growth and helps you stand out from the competition.
ISO 13485 not for you? Explore our range of QMS courses.
In a highly competitive industry, quality is everything.
SAE powers your growth and helps you stand out from the competition.
Trusted by Phillips Medical, Bayer, Baxter International, and other OEMs and suppliers large and small.
SAE offers on-demand and virtual training options, so you can choose the ISO option that fits your current work model. Complete the courses from anywhere, with no time limits constraining your learning pace.