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