Global Market Access

Regulatory Compliance of Telecommunication Devices

   Project Management 

Successfully complete your regulatory submissions in Brazil, Argentina, Mexico, Chile, Ecuador, Colombia and all countries in LATAM & Caribbean with local support. 

Regulatory and Quality Management System - Medical Devices 

Consulting

EU Medical Device Regulation (MDR), Clinical Evaluations Report (CER), CE Marking,Risk management, Corrective Action/Preventive Action (CAPA), RoHS & REACH Compliance.