Upcoming events

Switch to Calendar View

• CDISC: Creating CodeList Lookup Tables

  • When
    19 Sep 2018
  •  
    11:00 AM
  • Location
    webinar

  Register

  Do you need to review and confirm codelist values for several variables in SDTMs?  Codelists are list of unique values for key variables such as LBTESTCD.  Codelists need to be cross-referenced with control terms.  See CDISC page as reference.

  I will review SAS code to create a codelist lookup table.

  SAS Savvy Premium/University Members attend for free but still need to register. Non SAS Savvy Premium Members must pay $65. It's not too late to upgrade today to attend for free.   

  Computer and phone connections are required. Webinar will be recorded for on-demand viewin

  
  

  Show details
• Tracking Patient Summary of Response Changes

  • When
    17 Oct 2018
  •  
    11:00 AM
  • Location
    webinar

  Register

  Do you work on oncology studies and need to track changes in response values over time?  Would it not be nice to have a patient summary of each response so that you can monitor changes in response when it happens?

  During this training session, I will show how you can group response and study day to create unique key variables for grouping since grouping by response only will combine separate responses across study day into one response group.  Our objective is to record each block of response over time instead of just grouping all response.

  SAS Savvy Premium/University Members attend for free but still need to register. Non SAS Savvy Premium Members must pay $65. It's not too late to upgrade today to attend for free.   

  Computer and phone connections are required. Webinar will be recorded for on-demand viewin

  
  

  Show details
• Better CDISC Compliance Techniques result in faster Breakthrough Therapies

  • When
    14 Nov 2018
  •  
    11:00 AM
  • Location
    Webinar

  Register

  Attend this webinar to hear my PhUSE Keynote from Hyderabad, India in July.

  What starts as initial positive results from breakthrough therapies can blossom into a multi-center, international phase three clinical study over several years. Throughout the history of FDA and other federal health protection agencies, the mission has always been to expect high quality data and efficient review process. As we serve this industry either as pharmaceutical companies or CROs, our objectives are common. From start to finish, the journey that programmers and statisticians take should be guided with CDISC compliance, better use of programming techniques and technology, and high motivation to overcome data and analysis challenges to produce efficacy results that significantly improve patient outcome while reducing the risks.
  

  SAS Savvy Premium/University Members attend for free but still need to register. Non SAS Savvy Premium Members must pay $65. It's not too late to upgrade today to attend for free.   

  Computer and phone connections are required. Webinar will be recorded for on-demand viewin

  
  

  Show details