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CDISC: In Theory and In Practice

Next month, the Pharmaceutical Industry’s SAS User Group (PharmaSUG) will host its first one-day event entitled “CDISC: In Theory and In Practice” at the Pfizer conference facility near La Jolla,..

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Moving Management of Clinical Data Standards Out of the Stone Age

For the past decade, there has been more and more of a push toward clinical data standardization, and with the Prescription Drug User Fee Act (PDUFA) authorizing the FDA to mandate clinical trial..

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TransCelerate BioPharma to Address Clinical Data Standards

Last year was record setting for new drug approvals, with 39 new drug and biological products approved in the U.S., the highest number in 16 years. The prediction is for even more approvals in 2013. 

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d-Wise Technologies', SAS Partner, Presents/Sponsors PharmaSUG 2013

d-Wise Technologies Inc., a clinical optimization and technology leader and SAS Alliance Partner and CDISC Platinum member/Registered Solutions Provider based in Raleigh-Durham, NC is proud to be a..

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On the Eve of ADaM - Clinical Standards Update

d-Wise Sponsors PhUSE - Single Day Event-Durham 

PhUSE Raleigh-Durham SDE - Thursday, April 18thDuke Clinical Research Institute - Durham, North Carolina

This event will focus on issues related to..

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Setting New Clinical Data Standards for Parkinson’s Disease


Clinical Data Standards

An advancement in the fight against Parkinson’s disease (PD) was recently reported. The discovery was due to new clinical data standards. The standards allowed for a better..

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FDA/PhUSE 2013: A Working Group Overview

d-Wise Technologies will be participating at this year's FDA/PhUSE event in Silver Springs, MD. March 18-19.

The event will provide updates on collaborations with project groups to improve..

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WHITEPAPER: The Process & Governance of Implementing ADaM


Over five years ago, the CDISC ADaM standard was released as a set of principles and best practices for pharmaceutical research. The problem was the model was not really an industry..

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