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White Paper

Consistency, Control and Compliance white paper

Developing, executing and managing the transformation, analysis and submission of clinical research data with SAS® Drug Development

About this paper

In an industry shaped by ever-increasing regulation, global competition and market expectations, research-based biopharmaceutical organizations need ways to improve the efficiency and productivity of drug development processes. Traditional information management practices—constrained by manual data transfer, workflow and audit procedures—are not measuring up. This white paper describes SAS® Drug Development, which provides a unified platform for bringing consistency, control and compliance to information processes, from data aggregation through analysis and reporting to FDA submission.

Über SAS

SAS ist weltweit Marktführer im Bereich Analytics. Kunden an mehr als 83.000 Standorten setzen innovative Analytics-, Business-Intelligence- und Datenmanagement-Software und -Services von SAS ein, um schneller bessere Geschäftsentscheidungen zu treffen. Seit 1976 verschafft SAS Kunden rund um den Globus THE POWER TO KNOW. Weitere Informationen über SAS.

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