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1479 Search result(s):
E-Learning Course EU AI Act  
In this practical e-learning course, we provide step-by-step support to help you understand and implement the requirements of the EU AI Act.  
Seminar AI Act for Medical Device and IVD Manufacturers  
Learn how to implement the AI Act for your medical and IVD medical devices in a legally compliant and efficient manner, thereby avoiding compliance risks.  
Live Session AI-Supported Software Development  
Here, you can find out what AI coding tools can do in practice, what pitfalls they entail, and how you can handle them appropriately.  
Seminar ISO 42001 Integration  
Learn how to seamlessly integrate ISO 42001 into your ISO 13485 and ISO 27001 management systems in two half-days – with a ready-made project plan.  
MDR & IVDR Approval  
Bringing medical and IVD medical devices to the EU market quickly and compliant with the MDR and IVDR - from the approval strategy to post-market surveillance.  
MDR Expert Session  
Our one-hour MDR expert session will clarify the qualification of your medical device and the best approval strategy.  
Readiness Check  
Be on the safe side with our readiness check and accelerate your MDR/IVDR conformity assessment with a notified body.  
Change & Transformation Projects  
Consulting for medical device manufacturers regarding change and transformation projects – prepare your regulatory affairs department for tomorrow.  
Computerized Systems Validation  
We help you set up a lean CSV process to validate relevant computer systems and document them in a regulatory-compliant manner.  
International Approval  
International approval of medical devices: Bring your medical or IVD medical device to all markets in the world in a predictable and safe manner in accordance with all regulatory requirements.  
Results 311 until 320 out of 1479
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