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1502 Search result(s):
Person Responsible for Regulatory Compliance (PRRC)  
We take on the role of the Person Responsible for Regulatory Compliance (PRRC) according to MDR and IVDR and ensure your regulatory compliance.  
US Agent  
We are your reliable partner for legally compliant communication with the FDA and, as your US Agent, ensure your market access in the USA.  
In-country Representation  
We are your reliable authorized representative for medical devices in Europe and Switzerland, as well as your Responsible Person in the United Kingdom, and your US Agent in the USA, ensuring your…  
Podcast  
Our podcast keeps you well informed and allows you to talk to experts, auditors, and investigators on an equal footing.  
Johner Academy Book Demo  
Book your free & non-binding live demo for the Johner Academy now Our expert from the Johner Institute will guide you through the intuitive user interface and show you how you can gain confidence in…  
Seminar Risk Management and ISO 14971  
Learn how to coordinate the necessary risk management activities and create compliant documentation for your medical devices.  
Compact Seminar Requirements of the US FDA  
Learn about the basic requirements that the FDA imposes on the marketing of medical devices, which you and your company must know, understand, and fulfill.  
Advanced Seminar FDA Inspection  
This seminar helps you optimally prepare yourself for an FDA inspection. That way, nothing will stand in the way of a successful inspection.  
Seminar Medical Device Consultant MPDG  
We will enable you to fulfill your (new) role as a medical device consultant in accordance with the MPDG and competently implement the legal requirements.  
Compact Seminar Unique Device Identification (UDI)  
We help you navigate the regulatory jungle and label and register your medical devices in accordance with the MDR.  
Results 311 until 320 out of 1502
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