FREE CSPT Quality Assurance Protocols Questions and Answers
What is the main objective of quality assurance protocols in sterile compounding?
Quality assurance protocols are designed to ensure that CSPs are safe, effective, and of high quality.
What is a primary benefit of having a well-documented quality assurance program for sterile compounding?
A well-documented quality assurance program helps ensure compliance with regulations and standards, ensuring safety and quality.
What is the purpose of performing routine environmental monitoring in the compounding area?
Environmental monitoring helps identify contamination sources and ensures a sterile environment for compounding.
What is the significance of assigning beyond-use dates (BUDs) in quality assurance?
BUDs help ensure that CSPs are used within their stability and safety period.
Which of the following is a key component of a quality assurance program in sterile compounding?
Quality assurance programs focus on continuously monitoring and improving compounding processes to ensure high standards.
What should be done if a compounded sterile preparation fails a quality control test?
Failed CSPs should be discarded, and the cause of failure should be investigated to prevent recurrence.
Which document is essential for standardizing procedures and ensuring consistency in sterile compounding?
SOPs provide detailed instructions for performing tasks consistently and correctly in sterile compounding.
Why is it important to perform competency assessments for Compounded Sterile Preparation Technicians regularly?
Regular competency assessments help ensure that technicians are skilled and knowledgeable about current best practices in sterile compounding.
What is the role of a Compounded Sterile Preparation Technician in maintaining the integrity of the cleanroom environment?
CSPTs are responsible for following proper gowning and aseptic techniques to maintain a sterile cleanroom environment.
Why are endotoxin tests important in quality assurance for CSPs?
Endotoxin tests detect harmful endotoxins that can cause severe reactions in patients if present in CSPs.
What is a "media fill test" used to evaluate in the context of quality assurance?
Media fill tests are used to simulate the compounding process and evaluate the aseptic technique of personnel.