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Home Search results for "serious%20adverse%20events"

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Best Regulatory Affair in Delhi NCR. iv Recall Action Level: The level to which the recall...

2023-10-20T06:36:36

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1.8 Domestic price of the device in the currency followed in the country of origin. 1.9 L...

2023-09-13T05:15:38

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the permission holder shall inform the date of launch of medical device in the market to ...

2023-08-05T05:38:39

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(a) the manufacturer shall establish documented requirements for health, cleanliness and c...

2023-10-11T04:52:42

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7.2 Bio-compatibility: (i) The dossier should contain a list of all materials in direct or...

2023-09-16T04:43:15

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2.0 Device description and product specification, including variants and accessories 2.1 T...

2023-09-14T04:54:40

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2.0 Device description and product specification, including variants and accessories 2.1 T...

2023-09-13T05:26:51

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(1) "clinical investigation" means the systematic study of an investigation medical device...

2023-08-26T07:17:26

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(1) "clinical investigation" means the systematic study of an investigational medical devi...

2023-08-23T10:49:08

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