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Whitepaper

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CDISC
Case Study

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CDISC
Whitepaper

An international pharmaceutical company has a massive problem: critical research data from thousands of scientists in labs spread across the globe is trapped in tens of thousands of spreadsheets. Associates need to quickly find critical data on compounds, assays and…

CDISC
Whitepaper

Presenting A New Approach to Taming Biomedical Data Variety Tamr Field Engineer Timothy Danford, Ph.D., discusses how Data Variety — the natural, siloed nature of data as it’s created — is creating a bottleneck to biomedical data analytics. Rule-based, deterministic…

CDISC
Webinar

For most pharmaceutical companies, submitting clinical study data to the FDA is an expensive and time-consuming process. A study sponsor must collect data from different sources, extract it from proprietary file formats, transform it to conform to CDISC standards, organize…

CDISC
Whitepaper

Clinical Trial Data: Automated, Replicable CDISC Conversion Synopsis + IND and NDA programs necessitate recurrent submission of clinical trial data to regulatory agencies in specific formats. + Trial data is stored in a tangled web of standards, versions, and file…

CDISC
Webinar

Watch Now » For most pharmaceutical companies, submitting clinical study data to the FDA is an expensive and time-consuming process. A study sponsor must collect data from different sources, extract it from proprietary file formats, transform it to conform to…

CDISC