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1479 Search result(s):
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.  
Seminar Person Responsible for Regulatory Compliance according to Article 15 MDR  
In this seminar, you will learn about the tasks and duties of the PRRC and how to perform the role in the company in accordance with the requirements.  
Advanced Seminar 510(k) Premarket Notification  
In this seminar, you will learn about the FDA's 510(k) procedure and, using concrete examples and exercises, how to implement the requirements.  
Author Seminar Clinical Evaluation  
This practical seminar helps you, as an author, plan your clinical evaluation optimally, carry it out efficiently, and document it compliantly.  
Beginners' Seminar Clinical Evaluation  
We introduce you to the clinical evaluation process and show you how to review and assess clinical evaluation files in a targeted manner.  
Seminar MDR in Detail  
You will gain an overview of the most important regulatory requirements, relevant standards, guidelines, and best practices in Europe.  
Compact Seminar Medical Device Regulation (MDR)  
You get a compact overview of the most important requirements of the MDR and learn how to implement them efficiently and within the applicable transition periods.  
Seminar Post-Market Surveillance under MDR  
Learn about the regulatory requirements for post-market surveillance (PMS) and how to implement them in your company without unnecessary effort.  
Results 281 until 290 out of 1479
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