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Clinical Trials
In conjunction with specialist CRA/CRO consultants, we can assist you with:
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Developing a tailored Clinical trial strategy for your company's product(s).
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Applying Good Clinical Practice (GCP) principles to your clinical trial.
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Incorporating health economic data collection into your clinical trials so that you can save time in obtaining
reimbursement for your product.
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Designing and managing clinical trials.
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Writing submissions to ethics committees and regulatory authorities to conduct clinical trials in Australia,
the EU, the US and Canada .
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Writing documents for clinical trials such as clinical trial protocols, investigator brochures, CRF's, clinical
trial reports, etc.
- Liaison with ethics committees and regulatory authorities.
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