印度 IVD 进口许可证注册。

Inamdar Yashashri M
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引用次数: 0

摘要

印度是一个巨大的医疗器械市场,并且在过去几年中持续增长。印度制造商若要在印度进口任何医疗器械,必须获得注册证书和进口许可证。要在印度注册医疗器械,必须有 CDSCO 授权的印度代理。进口许可证注册需提交填写完整的 MD-14 表,获得的许可证将使用 MD-15 表。本次审查的重点是印度新医疗器械进口注册程序的相关法规,以及相关法规的最新修订。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Registration of Import License for IVD’S In India.
India is a huge market for medical devices and is constantly increasing last few years. The registration certificate and import license is mandatory for manufacturer of India who wishes to import any medical device in India. Indian Agent authorized by CDSCO is required for registering the medical device in India. Duly filled Form MD-14 is required to be submitted for import license registration and license obtained will be in Form MD-15. The review focuses on the regulations concerned to the registration procedures import for new medical device in India with latest amendments in the regulation concerned.
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