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Leads CDISC, the non-profit that sets the clinical trial data standards required by FDA and PMDA, including oncology-specific therapeutic area guides.
Chris Decker is President and Chief Executive Officer of the Clinical Data Interchange Standards Consortium (CDISC). CDISC develops global standards such as SDTM, ADaM and CDASH that structure clinical trial data for regulatory submission, along with therapeutic-area user guides for cancers including breast, prostate and lung. He previously held senior roles in clinical data science and standards implementation in industry.
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Shares the tags leadership, regulation.
Shares the tags leadership, regulation.
Shares the tags leadership, regulation.
Shares the tags leadership, regulation.
Shares the tags leadership, regulation.