02-22-2012 11:03 AM - edited 02-22-2012 01:35 PM
Thanks for joining our webinar, "Quality in Compounding: QA, QC, CQI with USP and Practical Applications" with Dr. Thomas Kupiec.
View the on-demand recording or download the slides.
Have a question for Dr. Kupiec? Post your question here and he will take your questions for a limited period of time.
02-22-2012 01:39 PM
Here are some questions from our live presentation:
Q: Can you recomend a specific QA monitoring procedure for CSP's to meet 797 guidelines?
Q: Is there a requirement to do end product testing on sterile products that are manipulated in a 797 compliant IV room using 797 B.U.D. recomendated dating?
Q: Any general rule of thumb to determine the number of units compounded before testing and how many?
Q: Do you consider repacking fentanyl into syringes or vials a low or medium risk procedure?