Training for ISO 13485 - Medical Device Industry

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.

Course Title	Course Info	At Your Location
Auditing
Internal Auditor Training for FDA Regulated Industries (ISO 13485 and ISO 9001)	Course Info	Quote
RABQSA Certified FDA Regulated Industries Lead Auditor (ISO 9001/ISO 13485)	Course Info	Quote
Implementing
Risk Management/Risk Analysis for Medical Devices	Course Info	Quote
Design Control for the Medical Device Industry	Course Info	Quote
Effective Corrective and Preventive Action for FDA Regulated Industries	Course Info	Quote
Quality System Regulation (QSR) for the Medical Device Industry	Course Info	Quote
Incorporating Supplier Quality Management Techniques in FDA Regulated Businesses	Course Info	Quote
Process Mapping	Course Info	Quote
Process Mapping (Canada session)	Course Info	Quote
Corrective and Preventive Action	Course Info	Quote
Corrective Action Video-supported Learning Program (VHS/DVD)	Course Info
Skills for Success for the Management Representative	Course Info	Quote
Skills for Success for the Management Representative (Canada session)	Course Info	Quote
Understanding
Understanding and Implementing the ISO 13485 Standard	Course Info	Quote
Executive Overview (Medical Device & Pharmaceutical)	Course Info	Quote
An Overview of the Electronic Records and Signature Rule - 21 CFR Part 11	Course Info	Quote
Understanding FDA Regulations for Combination Products	Course Info	Quote
Understanding 21 CFR 210 and 211	Course Info	Quote

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