In the current scenario of COVID-19, suction pump is considered as one of the critical products for immediate supply. But with the decline in the global supply chains of suction pump, meeting the demand right on time would be challenging.
To ensure the world sustain the ever-growing demand in this time of emergency, as a prominent suction pump manufacturer, you might be willing to market your product across the globe or to be specific in Italy. But do you know how suction pump is classified in Italy by the Directorate General for Medical Devices? How Italy regulates suction pumps?
Have all your questions answered regarding:
- Suction pump Registration/notification in Italy
- Directorate General for Medical Devices suction pump Regulations
In addition, some global health authorities have already expedited their Regulatory pathways for suction pump. The dynamic nature of those developments might require manufacturers to be more attentive on the regional Regulatory aspects, too. In such a case, streamline suction pump global market entry with the best of regional Regulatory information and structural Regulatory approach.
As a responsible Regulatory partner, Freyr has already started assisting clients to accelerate and fast track registrations/notifications of suction pump in Italy.