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Our regulatory consulting group is experienced in the development of positioning strategies, integrated planning, management, preparation of dossiers and submission to regulatory authorities for smooth transition and conduct of clinical research in India. Our experts are experienced in effective and diplomatic liaison with regulatory bodies. We ensure fast turn-around on regulatory documents and represent/ support you in meetings with regulatory agencies, for scientific advice.
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Review of protocol |
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Preparation and review of clinical trial applications/dossiers |
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Import licenses |
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Effective communication with regulatory authorities |
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Assistance with independent review board/ethics committee approval |
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| © 2008 Mithas Labs. All rights reserved. |
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