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3. As per the rules, for manufacture or import of new drugs, the manufacturers/ importer a...

2023-10-28T05:42:42

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5.6.2 Review input: The input to management review shall include information on— (a) resul...

2023-10-11T04:40:16

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PROVIDED that the requirement of Transmissible Spongiform Encephalopathies (TSEs) or Bovi...

2023-09-16T04:48:49

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(viii) when any major non-compliance is observed during audit by the notified body which m...

2023-09-11T05:06:07

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(f) the applicant shall provide for isolation of sick animals as well as animals under tes...

2023-08-28T05:22:24

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. Registration of medical device testing laboratory (1) Before grant of registration to an...

2023-08-10T05:44:39

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The composition of the inspection team referred to in sub-rule (1) shall be determined by ...

2023-07-20T05:16:43

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Review input: The input to management review shall include information on— Central Drugs S...

2023-07-04T05:01:00

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Medicinal substances: Where the medical device incorporates a medicinal substance, the dos...

2023-06-27T05:03:28

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