Training on developing and implementing a quality system compliant to ISO 13485. It covers Medical Device QMS Development and Implementation.
Training is via in person and pedagogical practices.
Training will allow trainees to gain knowledge and skills to understand medical device regulatory quality requirements and how to develop, deploy and implement a compliant and effective QMS for the medical device sector.
Training is of benefit to personnel in a quality, supervisory or management capacity including individuals with responsibility for quality system processes.
Training includes Documentation, Management, Resources, Product Realization, Planning, Risk Management, Auditing, Management Review, Improvement and Medical Device Regs.
