21 de marzo de 2023
Artículo técnico
Esté preparado para la nueva fecha límite de aplicación del Reglamento de Productos Sanitarios (MDR) de la UE
Does Your Labeling and Artwork Offer a Path to Compliance?
Compartir
In February 2023 the European Parliament recognized the critical need to mitigate the risk of shortages for patient safety by granting an extension for the new EU MDR to 2027 or 2028 depending on device’s risk class.
This passage means medical device manufacturers can now take advantage of this opportunity to properly and cost-effectively implement labeling solutions that offer a clear corridor to compliance.
Download the whitepaper to learn how to:
- Avoid recalls and non-compliance
- Adhere to cross-border regulations
- Automate, optimize and centralize labeling
- Enable fast, flexible label changes
- Ensure security and auditability
- Cloud
- Normativo
- MDR de la UE
- Cadena de abastecimiento
- Etiquetado de proveedores
- Administración de material gráfico
- etiquetado
- Seguimiento y ubicación