• d-Wise Delivers Clinical Solutions

    • SAS Drug Development (SDD)
    • SAS Clinical Data Integration (CDI)
    • SAS Clinical Standards Toolkit (CST)
    • entimICE

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    Clinical Solutions
  • Are you ready for changes to The Prescription Drug User Fee Act (PDUFA-V)

    The new review program established by the FDA to promote greater transparency and increased communication on the most innovative products reviewed by the agency.


    d-Wise can help:

    • Standardize Your Study Data and Metadata
    • Move You from Just “Readiness” to an Executable Strategy



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    CDISC Certified Partner
  • See a Video Demo of Reveal Clinical
    Enterprise Search In Action.

    Learn how d-Wise's enterprise search technology goes
    beyond horizontal search products.



    Watch the Demo
    CDISC Certified Partner
  • Enterprise Clinical Data Search Just Got Easier!

    Download our Whitepaper, “10 Tips on Getting Funding for our Web-based Search Solution” to find out how.


    Download Now

    or Learn More

    Reveal Enterprise Search
  • Healthcare Data Optimization Using Data-driven & Repeatable Processes.

    • Actuarial Analysis
    • Quality Assurance
    • Medical Management
    • Operational Data Marts
    • Data Warehouses
    • Business Intelligence Platforms


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    Healthcare Data Optimization

Data and Process Optimization Services for Life Sciences & Healthcare


Systems Implementation and Integration

Systems Implementation & Integration

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Standards Implementation Governance & Training

Clinical Standards Implementation Governance & Training

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Data Mapping - d-Wise

Data Warehouse and Metadata Solutions

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Process Optimization

Process
Optimization

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See d-Wise at these Upcoming Events

PhUSE SDE - Boston, Masachusetts
Thursday, June 20 | Boston | BiogenIdec, 15 Cambridge Center

DIA 2013 49th Annual Meeting: Advancing Therapeutic Innovation and Regulatory Sciences
June 23-27 | Boston, Massachusetts |Boston Convention and Exhibition Center

What d-Wise Clients are Saying

  • "Helped us Get to Market Faster..."

    After d-Wise implemented SAS Drug Development© to align our Global Clinical Trial Management program we were able to run trials, look at the data, understand what our compound is doing and be able to make better decisions making it easier to manage our portfolio of compounds and help us get them to market faster."

  • "Make better decisions..."

    With d-Wise, you can run trials, look at the data, understand what your compound is doing and be able to make better decisions and that will make it easier to manage our portfolio of compounds and will help us get them to market faster."

  • "Both SAS and d-Wise helped us..."

    understand what we were tackling. I was pleasantly surprised at just how good d-Wise was in explaining data integration to a group of non-developers. We went from communicating our requirements to having a first pass in the test phase in three to four months. It moved really, really quickly,” Randazzo said, adding that he felt d-Wise’s consultant, Chris Olinger, really helped optimize the solution."
    Joseph Randazzo, Manager of Actuarial Services


OUR PARTNERS

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