Understanding ISO 13485: Quality Management Systems for Medical Devices

Join our exclusive webinar designed for professionals in the medical device industry in the Middle East region, focusing on the essential ISO 13485 standard. This webinar will provide a comprehensive understanding of ISO 13485, its scope, key requirements, and the benefits of its implementation for quality management systems in medical devices.

Objective

This webinar aims to demystify ISO 13485, covering its scope, key requirements, and the strategic benefits of its implementation. Attendees will gain valuable insights into the practical aspects of ISO 13485 and how it aligns with key regulatory requirements.

Agenda

• Overview of ISO 13485: Why ISO 13485?
• Scope and Applicability of the Standard
• Key Requirements of the Standard
• Implementation Strategy
• Benefits of ISO 13485 Implementation
• Key Regulatory Requirements Aligned with ISO 13485
• QA Session

Target Audience

This webinar is specifically designed for professionals involved in the medical device industry in the Middle East, including regulatory affairs specialists, quality assurance managers, and senior management of medical device manufacturing & distributing companies in the Middle East. 

Secure your spot and register now!