An Israel-based manufacturer of non-invasive medical devices approached Freyr for Regulatory support in product listing and to act as a legal representative for the listing process of their devices in India. As the product was a multi-functional device, It’s classification and the listing process, which was a new pathway put forth by CDSCO were challenging.
How did Freyr provide end-to-end Regulatory support to overcome the challenges? How did the client achieve timely compliance with the CDSCO? Download the proven case study.
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