We leverage our technological expertise to bring the power of automation for your report preparation efforts. Clinical reports and documents are critical elements that form the foundation of vital decision-making related to the future of your drug development. With our automation capabilities, we not only make the process faster but also ensure accuracy for your final document.
ClinDocs handles the dependencies between multiple documents by establishing the relationship between multiple MS-Word documents. Through the relationships, downstream updates to any child document, section, or parts of the document are handled automatically without you having to make changes at multiple places. We also handle the dependencies on external documents. Such automation not only helps efficiencies of document updates but also reduces the possibility of manual errors significantly.
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Making Your Reporting Efficient & Effective
Manually creating reports can be time consuming, error-prone, and may impact the compliance and quality of your reporting. Through the power of automation and technological intelligence, we take away the pains of your reporting requirements.
ClinDocs helps companies to set-up templates for clinical trial protocol, synopsis, clinical study reports, and many clinical study documents. Our deep understanding of Microsoft architecture and associated technologies allows users to create dependencies between documents and automate the creation of these documents. In addition, the automation allows you to avoid costly protocol amendments and confusion at clinical trial sites by ensuring that any changes to your clinical studies are reflected in the report accurately without additional manual efforts.