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Tytus Technology Service LLC was founded in 2019 with a mission to provide specialized services and regulatory consulting to globe clients in dental, pharmaceutical, nutraceutical, dietary supplement and food industry.


Tytus Regulatory Strategy & Execution:  

What we do
Regulatory Strategy & Execution:  

Helping our clients selecting the best regulatory filing route (such as IND, NDA, ANDA, GRAS, NDIN) , then working with the clients to prepare dossiers and provide step-by-step guidance that leads to successful filing.

Toxicology Study Design : 

Supporting our client’s regulatory filing with appropriately designed study protocols, assisting and supervising preclinical and toxicology studies and guidance for study reporting.

Medical Device FDA Registration: 

Supporting our clients with the most appropriate regulatory filing, and compiling dossiers to file for FDA 510K, medical device, cosmetics, claims and labels compliance consulting. 

ADA Certification:  

  We have experience and networks with American Dental Association (ADA) to help your dental products getting the prestigious ADA seal of approval, to support your marketing globally with this prestigious certification. 

Independent Self-Affirmed GRAS Panel:  

We have expert resources to form independent GRAS panels to verify through scientific procedures that your product meets the “Generally Regarded As Safe" definition.

Preclinical Service:

We partner with many GLP labs in Europe, China, USA providing human cells, and animal cells for the prediction of toxic and long-term effects of agents on the human body and the environment. Our cell culture systems are important for your day-to-day work. Human and non-human hepatocytes are available as fresh or cryopreserved.

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