October 2017

Invitational Webinar: the Original Risk Evaluation Comparison

What is this?  - an interactive online event that offers you a once-in-a-lifetime opportunity to:

  1. quantify patient risk from medical laboratory ‘errors’ by submitting in your analytical & quality control processes
  2. validate your QC process against the ‘Prime Directive’ of Risk Management: “At the least, the ability of the QC procedures to detect medically allowable error should be evaluated." 
  3. examine risk metrics of up to 300 analytical processes
    1. mainly for glucose, calcium and sodium
  4. evaluate the value of a NEW approach to quality management in terms of:
    1. the number of patients you can potentially save from risk and
    2. the associated clinical/legal savings
    3. based on your risk drivers
  5. participate in discussions and surveys on reports
  6. co-author, post and discuss results


Who is invited?
Attendance is limited to 1st twenty people to register.  Invitations will be extended to 30 to 40:
a.    Laboratory professionals from large, small, specialized and general laboratories who attended the AACC BrownBag session “Evaluate acceptability of patient risk at monthly/regular QC review.”
b.    Researchers, consultants, colleagues, and “QC keeners” invited by Zoe Brooks, M.O.R.E. Quality™ Consultants.
c.    People who contact us through social media posts and would like to either participate or review the data for publication.   <span style="color: #0000ff; text-decoration: underline;">zoe@awesome-umbers.org</&#115;pan>