Course Description

This course provides in-depth knowledge of the ISO 13485:2016 standard, designed specifically for organizations involved in the life cycle of medical devices. It guides participants through the structure and requirements of the standard and shows how to implement an effective Quality Management System (QMS) that ensures product safety, regulatory compliance, and customer satisfaction. The training emphasizes risk management, regulatory requirements, process controls, and documentation practices aligned with medical device industry expectations.

What You’ll Learn

By the end of the course, you will be able to:

• Explain the purpose, structure, and clause requirements of ISO 13485:2016.

• Define the QMS scope and apply a process-based approach for medical device organizations.

• Understand risk management principles specific to medical device manufacturing and supply.

• Interpret and implement regulatory requirements within the ISO 13485 framework.

• Establish documentation, procedures, and controls for design, production, and traceability.

• Set up effective monitoring, measurement, and CAPA processes.

• Define roles, responsibilities, and training requirements for QMS support.

• Integrate supplier control and outsourcing management.

• Prepare documentation and records to demonstrate conformity and certification readiness.

• Build a roadmap for ISO 13485 implementation across the organization.

Who Should Attend

• Quality Managers and QMS Coordinators in medical device companies

• Regulatory Affairs Specialists

• Design and Manufacturing Engineers

• Internal Auditors and Compliance Officers

• Consultants supporting ISO 13485 implementation

• Any staff involved in medical device lifecycle management

Recommended

• Understanding of your organization’s medical device processes is helpful

• No prior ISO experience is required

• Familiarity with regulatory or technical documentation is beneficial