Want to get clinical trials designed, built & submitted, faster? Now you can, with our off-the-shelf clinical metadata repository and study automation platform. We’ve automated those labour intensive manual tasks – from study set up to submission. Build your standards and study library in a central MDR, then easily find, manage, and reuse content. Even import and reuse content from EDC and e-clinical systems to build studies much faster. You can design and build studies in the leading EDC systems. Quickly convert datasets to SDTM or ADaM. And easily make submission deliverables like define files, while conforming to CDISC regulations.
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