BelliStria is a modern consulting company. It offers a new concept of consultancy to its collaborators and its clients.. 

"The collaborators provides a costum-made work to satisfy clients"

For this:
- The clients select the best technical-consultants available on the market to have the premium results of the intended work. 

- The collaborators are fully informed about the missions and are presented to the clients only when they are approved by an internal technical team and motivated to support their clients. 

"At BelliStria, clients FIRST and collaborators FIRST"
All should be satisfied.. To complete a FANTASTIC work, together. 

BelliStria is specialized in niche activities in Quality and Regulatory Affairs for: 
- Drug Device combination 
Article 117 MDR, QMS according to the latest versions of pharmacetical/ Medical devices standards ISO 13485, Human factors studies... DHF for FDA submission... etc 

- Medical devices (MD/MD-IVD)
QMS according to international standard (ISO 13485..), MDR and international regulations.

-Pharmaceutical products (chemical and biological) 
Quality system management acoording to the latest version of the international standrads 
Regulatory submissions in Europe (EMEA under CTD format) and at international level

Etc ..

BelliStria

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