Writing funding bids involves a combination of good science, clear scientific communication and communication of impact, clinical and regulatory awareness, accounting for the strong possibility that the reviewer is informed, but not necessarily a specialist. In the selection examples indicated here, I was responsible for ensuring that these key objectives were reached while being responsible for writing key parts of the text (as indicated)
(I have written over 70 of these types of documents, most of which are still restricted via NDA/CDA)
Head and Neck Cancer Diagnostic Solution bid in which I wrote the following sections:
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Commericialisation plan
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Regulatory plan
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Clinical translation plan
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Standards integration requirements
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Relevance and impact
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State of the art
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Resources, assets and budget section
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Ethical and clinical requirements annexes
Drug Induced Liver Toxicity and Liver Cancer Diagnostic Solution bid in which I wrote the following sections:
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Commericialisation plan
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Regulatory plan
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Clinical translation plan
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Standards integration requirements
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Relevance and impact
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State of the art
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Resources, assets and budget section
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Ethical and clinical requirements annexes
Stem cell targeting medical product bid (endogenous and exogenous stem cells with biological or chemical entity based therapeutic products) in which I wrote the following sections:
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Commericialisation plan
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Clinical translation plan
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Relevance and impact
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Market sizing and targeting
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Resources, assets and budget section
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Ethical and clinical requirements annexes