Navigating the regulatory landscape for medical devices in the Middle East is essential for ensuring compliance, product safety, and market success.
Join Syed Atheeq, Lead Auditor at SGS Saudi Arabia, for an insightful session where he will break down regulatory requirements, their impact on quality management systems (QMS), and how to effectively integrate them into business operations.
This webinar is ideal for regulatory affairs specialists, quality assurance managers, and senior management in the medical device manufacturing and distribution sector.
Objectives
- Understand key regulatory requirements for medical devices in the Middle East.
- Learn the importance of compliance and its impact on business operations.
- Discover how to map regulatory requirements into QMS processes.
- Gain insights on updating procedures, establishing controls, and ensuring compliance.
- Explore tools, techniques, and best practices for ongoing monitoring and improvement.
Agenda
- Identifying & Mapping Regulatory Requirements in QMS
- Updating QMS Processes & Procedures
- Insights on Updated Processes & Procedures
- Monitoring, Review & Continuous Improvement
- Tools & Techniques for Effective Implementation
- Interactive Q&A Session
Target Audience: This webinar is designed for professionals in the medical device industry across the Middle East, including:
- Regulatory Affairs Specialists
- Quality Assurance & Compliance Managers
- Senior Management of Medical Device Manufacturers & Distributors
- Medical Device Consultants & Industry Experts
Language: English
Register here today!
