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(b) the intended user (lay person or professional); (c) a general description of the princ...

2023-09-16T05:31:26

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Description and specification, including variants and accessories of the in vitro diagnost...

2023-06-27T05:11:45

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The device master file should include the following device descriptive information:— (a) i...

2023-05-20T06:48:45

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SIXTH SCHEDULE (See rules 21, 22, 33, 34, 45, 47, 52, 53, 60, 67, 68, 75, 76, 80, 81, 86, ...

2023-04-25T05:11:42

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Illustration: Anticoagulant monitoring, diabetes management, and testing for C-reactive pr...

2023-09-09T08:56:26

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Risk analysis and control summary: The device master file should contain a summary of the ...

2023-06-27T05:36:21

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Illustration: Anticoagulant monitoring, diabetes management, and testing for C-reactive pr...

2023-06-23T05:57:05

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In vitro diagnostic medical devices for blood grouping or tissue typing (a) Subject to cla...

2023-05-18T06:21:06

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Prohibition of manufacture and sale of certain drugs and cosmetics.— From such date43 as m...

2023-04-19T10:26:08

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