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Comprehensive Services
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Protocol Development
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Draft unto Final Protocol
Designing Case Report Form and Subject Inform Consent
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The key to achieving successful clinical studies is the provision of well prepared and detailed study protocols. Whilst the essential core of a protocol should concern itself with study design and methodology in the context of pharmaceutical research and development. This document assumes an extremely important role in recording procedures associated with the entire study conduct with reference to ethical, regulatory and legal requirements.
Prodia the CRO offers you protocol development (including Case Report Forms (CRFs) and subjects Informed Consent).
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CRF & Subject Informed Consent
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Prodia the CRO provide CRF's design and informed consent's design/translations.
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