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Anti-Microbial Reusable Face Mask

Hand Sanitizer Registration/Notification in USA

In the current scenario of COVID-19, Hand Sanitizer is considered as one of the critical products for immediate supply. But with the decline in the global supply chains of Hand Sanitizers, 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 Hand Sanitizer manufacturer you might be willing to market your product across the globe or to be specific in the USA. But do you know how Hand Sanitizers are classified in the USA by the United Sates Food and Drug Administration (US FDA)? How US FDA regulates Hand Sanitizers?

Have all your questions answered regarding:

  • Hand Sanitizer License, Notification, Registration
  • US FDA Hand Sanitizer Regulations
  • Hand Sanitizer GMP as per the US FDA

In addition, some global health authorities have already expedited their Regulatory pathways for Hand Sanitizers. The dynamic nature of those developments might require manufacturers to be more attentive on the regional Regulatory aspects, too. In such a case, streamline Hand Sanitizer’s 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 critical products for COVID19 - like Hand Sanitizers.

  • Sanitizer | Hand Rub For a different country?

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