Support for ISO 13485 and FDA Regulated Industries
SAI Global's comprehensive ISO 13485 and regulatory support program for the Medical Device Industry enables your organization to implement an effective ISO 13485 quality management system and meet domestic and international regulations for medical device, while achieving overall business improvement.
SAI Global is proud to have earned a 98.9% customer satisfaction rating on training courses conducted in the United States and Canada.
Contact Us!- Phone: Contact our Customer Service team at 1-800-374-3818.
- Email: Email our Training team at training.us@saiglobal.com.
- To Register Online: Click your preferred course above and select a date from the course page.
Call or email us today with no obligation.
Our ISO 13485 training courses include ISO 13485 training for implementation, ISO 13485 training for internal auditors, and lead auditor training for FDA regulated industries.
"What I really took away from this course is a much better understanding of the medical device industry system, nationally and internationally. I'm new to this industry so this course was a very good introductory course to quality system management."
--Lucy Kong, Boston Scientific Corp, Target Therapeutics
