{ Medical and Scientific Writing }
The DaVita Clinical Research (DCR) Medical Communication team applies therapeutic expertise and a commitment to quality to ensure scientifically accurate documents that are fully compliant with regulatory requirements. Writing and editing services are available as part of a full drug development program, a clinical trial, or a la carte. All documents are subject to a continuous quality control review to guarantee compliance with style guides and all applicable International Conference on Harmonization (ICH) standards and ICMJE Uniform Requirements.
Significant knowledge in the preparation of highly-specialized documents results in clearly executed reports that can help smooth the submission process.
In addition to assistance preparing studies for publication or presentation, the DCR Medical Communication team is available to help you with the development of:
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Preclinical and scientific reports
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Phase I-IV protocols
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Integrated clinical statistical reports
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Global clinical trial applications
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Drug, device, and biologics marketing applications
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Investigator brochures
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Pre-marketing and post-approval annual reports
