Date: 22th and 29th of August 2024
Time: 14:00h - 17:00h CEST | 9am - 12am EST
Location: Virtual
Language: English
Costs: € 895,- | $ 970.-
Introduction:
Are you ready to enhance your quality management skills? Join our ISO 13485 training program, designed specifically for aspiring and junior professionals in the medical device industry!
ISO 13485 isn’t just another standard; it's the heartbeat of quality management systems for medical devices worldwide. This globally accepted framework sets the gold standard for ensuring product safety, reliability, and compliance with regulatory requirements.
In an industry where adherence to regulations are crucial, mastering ISO 13485 is essential for success. It provides a strong foundation to navigate complex regulatory environments, including the EU-MDR, MDSAP, global medical device regulations, and the FDA’s evolving requirements.
By participating in this training, you will gain:
✅ An understanding of ISO 13485 principles and requirements
✅ Practical insights to streamline quality management processes
✅ Confidence to navigate regulatory audits and inspections
Whether you’re starting out in quality management, regulatory Assurance or looking to deepen your expertise, this training is tailored for your success. If you're dedicated to ensuring the safety and effectiveness of medical devices, this is your opportunity to make a significant impact!