Nirma University
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us fda documentation and regulatory writing drug regulatory affairs prior approval supplement pas patents para 4 regulatory ipr gmp quality management system regulatory affairs capa qms ghtf sg3
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GHTF study group 3

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Prior Approval Supplements (PAS)

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Regulations for drug approval in USA, E.U & India

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us fda documentation and regulatory writing drug regulatory affairs prior approval supplement pas patents para 4 regulatory ipr gmp quality management system regulatory affairs capa qms ghtf sg3
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