##  [Regulatory Services for Registration of Low Moderate Risk Devices in India](/case-studies/regulatory-services-for-registration-of-low-moderate-risk-devices-in-india) 

- [Medical Devices](/case-studies-main-categories/medical-devices)
- [Market Access](/case-studies-main-categories/market-access)





[CDSCO](/case-studies-heath-authority/cdsco)

 

 ![Regulatory Services for Registration of Low Moderate Risk Devices in India]()

A US-based medical device company specialized in manufacturing general hospital products was aiming to launch their products in the Indian market. The devices were manufactured at different manufacturing sites and each device was diversified with multiple components and different working principles. Owing to the pandemic, the regulations for devices in scope and the CDSCO review timelines were prolonged. In addition, the devices were due for regulation and the SUGAM portal and the CDSCO licensing portal were not accepting the applications.

Amidst all the challenges, how did Freyr manage to provide end-to-end product registration services for the client with quick TAT. Read through the proven case study.



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