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 take your quality management skills to the next level? Join us for this ISO 13485 training program tailored for aspiring 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 precision and compliance are paramount, mastering ISO 13485 is your ticket to success. Not only does it provide a solid foundation for navigating complex regulatory landscapes, but it’s also the key to unlocking opportunities in the EU-MDR, other global medical device regulations and even FDA’s evolving regulatory framework.
You will Gain:
✅ In-depth understanding of ISO 13485 principles and requirements
✅ Practical insights to streamline quality management processes
✅ Confidence to navigate regulatory audits and inspections
✅ Competitive edge in a rapidly evolving industry landscape
Whether you're a budding quality professional, a seasoned industry expert, or anyone in between, this training is designed with your success in mind. If you're passionate about ensuring the safety and efficacy of medical devices, this is your chance to make a meaningful impact!
Ready to elevate your career and make a difference in healthcare quality? Let's embark on this transformative journey together!