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 Ireland. But do you know how Hand Sanitizers are classified in the Ireland? How the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products (URPL, Polish: Urząd Rejestracji Produktów Leczniczych) give licences to Soaps/Hand Sanitizers? What are the licence requirements for soaps?
Have all your questions answered regarding:
- Hand Sanitizer Notification/Registration in Poland
- URPL Hand Sanitizer/Soap Regulations
- License Requirement for Soaps
- Soap Registration Guidance
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 Hand Sanitizers in Poland.