Note: The blog is excluded from the website search. If you want to search for something in the blog, you must use the blog's search function. Please contact us if you cannot find the information you are looking for using either the navigation or the search function. We will be happy to help you.

Results

For the search term: "..."

1499 Search result(s):
Feedback of our Customers: Melanie Henze, Preventicus GmbH  
Melanie Henze, Preventicus GmbH With the help of the Auditgarant, we were able to successfully complete our MDR approval compliance process. We are grateful for the high-quality templates and…  
Feedback of our Customers: Matthias Hippe, Mediceo GmbH  
Matthias Hippe, Mediceo GmbH As a young company without much background in the field of regulatory requirements for medical devices, we were faced with the major challenge of creating the framework…  
Feedback of our Customers: Anja Discher, DISCHER Technik GmbH  
Anja Discher, DISCHER Technik GmbH We are very happy that we did so well in our MDR audit. The auditor said that this is very rare. Investing in the Auditgarant was well worth it! Many thanks to the…  
Feedback of our Customers: Sabine Dörner, EyeSense GmbH  
Sabine Dörner, EyeSense GmbH The Johner Institute's Auditgarant was a great help with our first submi­ssion. Thanks to the e-learning, the comprehensive templates, and the always helpful team, we…  
Feedback of our Customers: Max Power Life Science GmbH Team  
Max Power Life Science GmbH Team We are a newly founded com­pany striving for ISO 13485 certification. First of all, the Johner Institute's Auditgarant convinced us. In an industry subject to strict…  
Rate Us  
We use Trustpilot as an independent review portal Please let us know how satisfied you were with our consultants and products. We would be very grateful if you could take a moment to write a review…  
EN_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.  
EN_Seminar Risk Management and ISO 14971  
Learn how to coordinate the necessary risk management activities and create compliant documentation for your medical devices.  
EN_Seminar FDA’s Quality Management System Regulation  
This seminar will help you understand the FDA's new requirements for your quality management system and implement them in your company successfully.   
EN_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.  
Results 121 until 130 out of 1499
X

Privacy settings

We use cookies on our websites. Some of them are essential, while others help us to improve this website and your experience.