In the current scenario of COVID-19, laryngoscope is considered as one of the critical products for immediate supply. But with the decline in the global supply chains of laryngoscope, 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 laryngoscope manufacturer you might be willing to market your product across the globe or to be specific in India. But do you know how laryngoscope is classified in India by the Central Drugs Standard Control Organisation (CDSCO)? How CDSCO regulates laryngoscope? How different types of laryngoscopes are classified?
Have all your questions answered regarding:
- Laryngoscope Registration/notification in India
- CDSCO Laryngoscope Regulations
In addition, some global health authorities have already expedited their Regulatory pathways for laryngoscope. The dynamic nature of those developments might require manufacturers to be more attentive on the regional Regulatory aspects, too. In such a case, streamline laryngoscope 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 laryngoscope in India.