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.

Understanding Courses	Info	Agenda	Public	In-House	Base Price	Early Bird
ISO 13485 - Understanding and Implementing Course			Register Now	Request Quote	$1,095
Implementing Courses	Info	Agenda	Public	In-House	Base Price	Early Bird
Risk Management/Risk Analysis for Medical Devices Course			Register Now	Request Quote	$1,095
Design Control for the Medical Device Industry Course			Register Now	Request Quote	$1,095
Corrective and Preventive Action (CAPA) for FDA Regulated Industries Course			Register Now	Request Quote	$1,095
Quality System Regulation (QSR) for the Medical Device Industry Course			Register Now	Request Quote	$1,095
Process Mapping Course			Register Now	Request Quote	$995	$846
Corrective and Preventive Action (CAPA) Course			Register Now	Request Quote	$495	$421
Actions Correctives/Actions Preventives (CAPA) En Français			Register Now	Request Quote	$495	$421
Enhancing Management Representative Skills to Support Organizational Success Course NEW!			Register Now	Request Quote	$1,200	$1,020
Auditing Courses	Info	Agenda	Public	In-House	Base Price	Early Bird
ISO 13485/ISO 9001 - FDA Regulated Industries - Internal Auditor Course			Register Now	Request Quote	$1,095
ISO 13485/ISO 9001 - FDA Regulated Industries - Lead Auditor - RABQSA Certified Course			Register Now	Request Quote	$1,995