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| Clinical Research Outsourcing |
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| Cadila Pharmaceutical's Clinical Research Organization provides the client with scientific, medical and regulatory support for Bioequivalence and Bio-analytical studies; Formulation Development; in addition to protocol design and development, implementation, data collection and reporting. Through years of global compliance experience, Cadila's CRO Team consistently meets competitive timelines and exceeds regulatory compliance standards. Cadila's CRO Team routinely performs BE/BA studies and/or dossiers to: ANVISA (Brazil ), DCGI ( India ), MHRA (U K), MCC ( South Africa ), WHO ( Geneva ), TGA ( Australia ), and is compliance certified under ISO 9001 and ISO 14001. |
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