- Elaboration and assembly, attendance, protocols for obtaining of: 
 
. Company´s Authorization of operation in the area of health products.  

. Operation authorization for medicines and common pharmaceutical goods subject special control. 

. Operation authorization for drugstores. 
 
- Registration of health products (medical Products, equipments and diagnosis in vitro). 
 
- Registering of products for the health (medical Products, equipments and “in vitro” diagnosis). 
 
- Express Protocols (ANVISA Protocol in up to 24hs after the document reception). 
 
- Auditing and consultancy for manual development and certification in Good Practices of Production and Control and Good Practices of Storage and Distribution (Distributor and Importer). 
 
- Site with restricted access to each customer with database for consultation of process status, updated daily with documents and files with ongoing process at ANVISA. Page for process consultations.