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Case Study 1: U.S. Endotracheal Tube Manufacturer

Case Study 1: U.S. Endotracheal Tube Manufacturer – Achieving 21 CFR 820 Compliance & 510(k) Submission with Medfins International. Client BackgroundThis case study focuses on a U.S.-based medical device manufacturer…

MD-27 Permssion

MD-27 Permssion PurposeMD-26 is the application form used to seek permission from the Central Licensing Authority (CLA) to import or manufacture a new medical device in India.“New” means a medical…

The Role of Indian Authorized Agent in Medical Device Industry

The Role of Indian Authorized Agent in Medical Device Industry The medical device industry in India has undergone significant transformation and growth over the past few years. This growth is…

Case Study 1: U.S. Endotracheal Tube Manufacturer

MD-27 Permssion

The Role of Indian Authorized Agent in Medical Device Industry

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