Medical device manufacturers seeking market authorization in Peru must register with the Dirección General de Medicamentos, Drogas e Insumos (DIGEMID), a unit of the Peruvian Ministry of Health.
Let Emergo assist you in evaluating the Peruvian medical device regulatory framework as it applies to your device(s)
Emergo's worldwide network of consultants, industry contacts and regulatory sources allows us to provide incisive analysis of multiple medical device markets, including Peru. Our Global Regulatory Overview report service on Peru provides in-depth coverage of the following topics:
- DIGEMID Regulatory Background
- Product Assessment
- Authorized Representation in Peru
- Medical Device Registration Requirements
- Costs and Timeframes
- Labeling and Language Requirements
- Regulatory Roadmap for Peru
Please contact us for more information about our Regulatory Overview Report for Peru.