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