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