In the current scenario of COVID-19, Goggles (Protective) are considered as one of the critical products for immediate supply. But with the decline in the global supply chains of protective goggles, 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 protective goggles 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 protective goggles are classified in the USA by the United States Food and Drug Administration (US FDA)? How US FDA regulates protective goggles?
Have all your questions answered regarding:
- Goggles (protective) Registration/notification in the USA
- US FDA Goggles (protective) Regulations
In addition, some global health authorities have already expedited their Regulatory pathways for goggles (protective). The dynamic nature of those developments might require manufacturers to be more attentive on the regional Regulatory aspects, too. In such a case, streamline protective goggles’ 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 protective goggles in the USA.