Requirements

• You should be familiar with quality management systems or have prior experience in the medical device industry

Description

Who this course is for:

• Quality managers
• quality assurance officers
• and quality control personnel responsible for ensuring compliance with ISO 13485 and maintaining a robust quality management system.
• Regulatory affairs professionals responsible for understanding and implementing regulatory requirements for medical devices and ensuring compliance with ISO 13485.
• Engineers and designers involved in the design and development of medical devices
• who need to understand the specific quality management requirements outlined in ISO 13485.
• Compliance officers and internal auditors who are responsible for auditing and verifying adherence to ISO 13485 standards within their organization.
• Individuals working in medical device manufacturing companies
• suppliers
• or contract manufacturers who need to ensure their operations align with ISO 13485 requirements.
• Consultants and advisors who provide guidance and support to organizations in implementing ISO 13485 and establishing effective quality management systems for medical devices.
• Individuals who wish to enhance their knowledge and skills in quality management systems for medical devices to advance their career prospects in the medical device industry.