400-876-8783
服务热线:
印度器械注册
Medical Device Registration Certificate in Form 41 (For Foreign Manufacturer)
· Determine your device fits or not into the list of notified Medical Devices regulated under Drugs and Cosmetics Act, 1940; and Rules, 1945.
· Coordinate the device registration and approval process with Indian Medical Device Regulators (DCG(I)/CDSCO)
· Preparation of all necessary documents for the product registration application including Forms 40.
· Suggesting appointing an Indian Agent as your official representative.
· Submission of Site Master File and Device Master File as needed。
· Coordinate with the DCG(I)/CDSCO to address follow up questions and monitor progress

邮箱:info@sungoglobal。com


服务热线: 400-876-8783  

     021-68828052


联系我们contact us
棋牌游戏平台 网络棋牌游戏 手机棋牌游戏 开元棋牌 棋牌游戏平台 亲朋棋牌 手机棋牌游戏 波克棋牌 娱乐棋牌 三多棋牌