About me


My career in the medical device field is spanning more than 25 years. During this time, I have been able to gather a wide range of experience in many different fields.




For several years, I examined and tested a wide variety of materials and products in the laboratory. Biocompatibility and functionality of the products played the most important role.


Furthermore, I carried out the toxicological assessment of the materials, up to the assessment of the regulatory requirements for later use in humans. I was able to gain international experience in a wide range of cultures across national borders and thus move safely around the world.

 


This is particularly helpful in the area of auditing, because here it is necessary to bring together all the requirements worldwide and to always do justice to the pharmaceutical industry with its complex regulatory circumstances.

 


 

Conrad Julius Inhaber der Julius-Consulting bietet weltweit Technische Dokumentation von Medizinprodukten Marktüberwachung und Validierung von Medizinprodukten




Conrad Julius Inhaber der Julius-Consulting ist Risikomanager für Medizinprodukte Medizinprodukte-Richtlinien zuständig



 

My work at TÜV Rheinland as an expert for the biocompatibility of medical devices was also beneficial. Here I was able to gain insights and experience in the exciting world of notified bodies, as well as build and expand the necessary network.

 


I have been moving in the exciting and thrilling world of GMP audits since the summer of 2020. I can look back on more than 50 audits carried out worldwide. The focus was on the DACH region, but I was also able to gain experience in North America, Iceland, Turkey, Taiwan and India.

 

 


Finally, my 7 years of experience in the pharmaceutical world as a toxicological expert at Merz Pharamceuticals GmbH from 2007 to 2013 also helped me a lot.