ISO 13485:2016 – Medical Devices Quality Management System: Key Requirements and Implementation

This webinar provides an overview of ISO 13485:2016 and its role in establishing an effective quality management system for organizations involved in the medical device industry. Participants will explore the standard’s key requirements, risk management principles, and relevant regulatory considerations throughout the medical device life cycle.

By the end of this webinar, participants will be able to:

• Understand the purpose and importance of ISO 13485:2016.
• Identify the key requirements of the standard.
• Understand the quality and regulatory requirements applicable to medical devices.
• Recognize the benefits of implementing an ISO 13485-compliant quality management system.

Agenda

• Introduction to ISO 13485:2016
• Structure and key requirements
• Risk management and regulatory considerations
• Quality management throughout the medical device life cycle
• Certification and implementation overview
• Q&A

Target Audience: This webinar is recommended for:

• Medical device manufacturers and suppliers
• Quality Assurance and Quality Control professionals
• Regulatory Affairs professionals
• Medical device engineers
• Quality auditors and consultants
• Professionals involved in medical device quality management

Language: Arabic

Cost: No Charge