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Whereas the draft of the Medical Devices Rules, 2016 was published, as required under sub...

2023-08-26T07:09:19

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Whereas the draft of the Medical Devices Rules, 2016 was published, as required under sub...

2023-08-18T04:30:39

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Whereas the draft of the Medical Devices Rules, 2016 was published, as required under sub...

2023-08-14T05:13:56

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Whereas the draft of the Medical Devices Rules, 2016 was published, as required under sub...

2023-07-13T09:06:38

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15.However, detailed guidance documents should be prepared providing the requirements and ...

2023-10-28T05:49:46

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3.16 Rework means action taken on a non-conforming product that will fulfill the specified...

2023-10-09T05:44:44

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16.0 Claimed Shelf life: This section should provide information on stability testing stud...

2023-10-05T05:30:04

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16.0 Claimed Shelf life: This section should provide information on stability testing stud...

2023-10-04T04:43:45

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Where the Central Licensing Authority or the State Licensing Authority has reason to beli...

2023-07-20T05:08:14

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