Brazil Medical Device Registration Services

DDReg Pharma provides comprehensive regulatory consulting for medical device registration within the Brazilian ANVISA framework. They offer essential services including risk classification, dossier preparation, and Brazilian Good Manufacturing Practices (BGMP) support. The company acts as a local Brazil Registration Holder (BRH) to fulfill mandatory legal representation for foreign manufacturers. Their expertise extends to post-market surveillance, labeling compliance, and full lifecycle management in the Brazilian market.