In the current scenario of COVID-19, self-inflating bag is considered as one of the critical products for immediate supply. But with the decline in the global supply chains of self-inflating bag, 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 self-inflating bag manufacturer, you might be willing to market your product across the globe or to be specific in the USA. But do you know how self-inflating bag is classified in the USA by the United States Food and Drug Administration (US FDA)? How US FDA regulates self-inflating bag?
Have all your questions answered regarding:
- Self-inflating bag registration/notification in the USA
- US FDA Self inflating bag Regulations
In addition, some global health authorities have already expedited their Regulatory pathways for self-inflating bag. The dynamic nature of those developments might require manufacturers to be more attentive on the regional Regulatory aspects, too. In such a case, streamline self-inflating bag 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 self-inflating bag in the USA.