www.d-Wise.com

  • Increase font size
  • Default font size
  • Decrease font size
Home Company News
News

d-Wise Builds Actuarial Data Warehouses in Health Insurance

E-mail Print PDF

A quote from Joseph Randazzo, Manager of Actuarial Services at Excellus BlueCross BlueShield:

“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.

Click here to read the full press release from SAS: http://www.sas.com/success/pdf/excellus.pdf

Is data integration enabling analytics within your organization?

 

FDA Provides Clear Message for CDISC Standards, Challenges Still Exist

E-mail Print PDF

Today, on the CDISC Blog, Dr. Kush, the President of CDISC, put to rest a few years of confusion over the direction of CDISC standards within the FDA.

Over the last 3 years, since the release of the PDUFA IT Plan, the industry has been in a state of confusion with no clear understanding of how to move forward with the adoption of CDISC standards.  Messages were being distributed that the FDA was moving to an HL7 xml type message and SAS transport files would disappear by 2013.  This was never more evident at the CDISC interchange last November when every speaker gave an impassioned plea to the FDA panel to give the industry a clear message.

Dr. Kush provides a very optimistic outlook by clearly stating the FDA is stating that all data submitted in CDISC standards and SAS transport and define.xml are the standard formats for the foreseeable future.   This is great news for the industry as a whole as we now have a clear understanding of the expectation of our regulatory partners.  This news, combined with the creation of the Computational Sciences division at the FDA focused on defining and delivering around data standards and technology, provides us with a light at the end of the proverbial tunnel.  The inaugural CDER/CBER Computational Sciences Annual Meeting on March 22 is one more step to support a clearer focus.

With no intentions of throwing a wet blanket on this wonderful news, challenges still exist.  Companies still struggle with the cost and efficiency of using the CDISC standards.  They struggle with the need to submit data in a standard format vs. the ability to use the standards operationally.  The FDA is working through the challenges of adopting the standards when it doesn’t meet all their needs and doesn’t yet support the nuances of specific therapeutic areas.  These are challenges which are very real and hard to overcome in some cases.

However, while these issues still exist, having a clearer direction agreed upon by both CDISC and the FDA, we can move forward as an industry and push through the challenges we all face.  d-Wise is excited about the opportunity to help our customers implement and adopt the CDISC standards.

 

 

d-Wise Hosted Webinar on Extending SAS Drug Development

E-mail Print PDF

SAS Drug Development provides an information repository allowing users across an organization to collate, manage, and analyze their clinical data and other artifacts within a centralized and compliant platform. While SAS Drug Development offers a wealth of functionality it does not necessarily provide answers to every business process. However, SAS Drug Development does provide a very extensible platform allowing for a variety of methods for extending the capabilities of the solution to meet your business needs.

This webinar provided an overview of the technical options for extending SAS Drug Development, a summary of case studies where efficiencies were gained, and a demonstration of sample prototypes using the extensibility of the solution.

You can access the recorded webinar and associated slides by creating a new account and logging into our site.  Once you register and log in, you can download webinar content from our downloads page.

 

Clinical Data Warehouse: A Brief Introduction and Examination of Industry Business Requirements

E-mail Print PDF

Webinar Invitation

d-Wise recognizes that companies are faced with larger and larger quantities of data spread across multiple "data silos" and the associated challenge of how to get the most value from their data. This challenge is multiplied as organizations go through mergers and acquisitions and face an increased number of diverse systems containing valuable information.

Pharmaceutical companies are beginning to understand that clinical or operational data warehouses help meet the need to look closely at data and metadata as part of the solution, and address a number of challenges. These challenges include the move away from internal standards towards well established external standards, how a standard data model might be extended to meet their requirements, and building views or data marts for consumption of this data.

This session will provide the following:

  • A basic understanding of a data warehouse
  • An examination of the variety of standards based options for data warehouses
  • An overview of the general business requirements faced by industry in moving data from silos to a centralized data warehouse
  • Initial assessment of the standards based options with respect to a variety of general business requirements

Please join us for this webinar on October 15 from 11am to noon EST. Please go the following link to register for the event. The event is limited to 90 participants so register early.

https://www.livemeeting.com/lrs/8001420460/Registration.aspx?pageName=33jmxx2kvmhwff03

Note: the web meeting will use Live Meeting and will prompt you for an installation. You can select the web only option and do not have to install any components. The conference call number is a US toll number.

 

d-Wise to Attend and Present at PhUSE

E-mail Print PDF

d-Wise Consultants will be attending the annual PhUSE (www.PhUSE.eu) conference in Basel, Switzerland from October 19-21. This is the premier conference in Europe for Pharmaceutical Software Users.

In addition, d-Wise Consultants will deliver presentations on a variety of topics including:

Chris Decker, Life Sciences Director will present “The CDISC/FDA Integrated Data Pilot: A Case Study in implementing CDISC Standards to Support an Integrated Review”. This presentation will provide an update on the Pilot project and a discussion of the lesson learning in implementing the newest CDISC standards and using those standards to integrate data.

Stephen Baker, Senior Consultant, will present “Crossing the Chasm: Simplifying Data Management with Perl and Metadata”. This presentation will discuss how Perl was applied to the challenges of supporting data from multiple vendors with unique activities and breaking those activities down into “actions” – and driving those actions with object-oriented metadata, using tools to separate business logic from programming logic, and rapidly building capability through automated processes.

Chris Decker will also present “ETL and the Clinical Programmer – They don’t have to be Enemies!” This presentation will discuss the challenges of understanding and implementing a traditional ETL process within the clinical programming environment and provide a case study of implementing an ETL solution.

 
  • «
  •  Start 
  •  Prev 
  •  1 
  •  2 
  •  3 
  •  4 
  •  Next 
  •  End 
  • »


Page 1 of 4