Trademarks

The following are trademarks of Propper Manufacturing Co., Inc.
Accucharge Fidelatone PowerAll Steri-Stik
Alert-O.A.D. F/O (Fiber Optic) Precisometer Steri-Wrap
Arrowhead Gas Chex Propper Plus Strate-Line
Autofoc Glaucotest Propper Star Superlume
Autosfig Hi-Dri Push-Button Temptube
Bev-L-Edge Hi-Speed Quick Challenge Ternopil
Bio-Challenge Test Pak Irrigo Quikuff Test-Pak
Bi-Ok Lifo Seracult Timecard
Cal-Mark LoT; Chex-All Seracult Plus Trophy
Cardiouet Lumicyte Seraket Twindicator
Champion Magnalume Sera-Sharp Twin-Frost
Chex-All O.K. Sera-Slide Ultra
Duo-Check Once-A-Day Sera-Sphyg Vaporline
Duo-Flash Once-A-Day Test Pak Serature Velket
Duo-Record Oscillotonometer Smalstrip
Duo-Spore Pak-Rak Spiraflex
EO Easy Read Pass/Fail Steri-Dot

Latest Courses

Propper Academy Connects with Sarah B. Cruz on Strategic Networking

Propper Academy Connects with Sarah B. Cruz on Strategic Networking

Live Conversation on Friday, April 12th at 2PM ET

Maximizing Your Experience at the HSPA Annual Meeting

We will discuss strategic networking at the HSPA Annual Meeting and beyond. The formal education at the conference is valuable but the conversations with fellow technicians, suppliers, and other industry allies make the conference the best opportunity for professional growth each year!

Don’t miss this opportunity to connect, learn, and elevate your networking skills as a Sterile Processing Technician. Register now for an enriching experience at Propper Academy Connects.

ON DEMAND: What’s Wrong with this Picture? Identifying Common Mistakes in SPD

What's Wrong With This Picture? Identifying Common Mistakes in SPD

Discover the essentials of achieving excellence in Sterile Processing—a critical aspect of patient safety gaining increased attention from surveyors, healthcare administrators, and legislators nationwide. This presentation is an interactive exploration, challenging you to identify the top 20 commonly overlooked issues within the Sterile Processing Department. Join us to enhance your understanding of industry best practices and sharpen your analytical skills alongside Infection Preventionist peers. Uncover these key issues for improved operational efficiency and elevated standards in patient care.

Objectives:

  • Identify and recall the key industry best practices in Sterile Processing.
  • Explain the increasing importance of instrument reprocessing in healthcare facilities.
  • Propose solutions for enhancing operational efficiency in response to identified issues.
  • Analyze the implications of overlooked issues in Sterile Processing on survey reports and healthcare administration.
  • Develop a comprehensive plan for addressing and preventing commonly overlooked issues in Sterile Processing.

This course is approved to receive 1.0 CE from CBSPD and HSPA.

ON DEMAND: But Is It Really Clean? Challenging the Status Quo For How Our Industry Approaches Process Monitoring

But Is It Really Clean? Decontamination, Processing Monitoring and Verification

 

If it’s not clean, it can’t be sterile…right? Even though this industry mantra is widely shared and discussed, there is an aspect of the discussion that is ripe for further consideration. While the industry has been rapidly moving toward more and more adoption of monitoring every sterilization load with a biological indicator (BI), the same cannot be said of process monitoring for our mechanical washers and disinfectors. While daily monitoring of mechanical washers with process challenge devices (PCDs) is common practice in Sterile Processing departments, what happens when a failure is detected? What should happen? And why are we not testing every washer load the way we test our steam sterilization loads? This presentation hopes to provide a catalyst for this important industry conversation.

 

Objectives:

  • Discuss the purpose and requirements of processing monitoring for mechanical washers and disinfectors.
  • Compare the process monitoring practices of biological indicators (BIs) and cleaning PCDs.
  • Outline how the current industry conversations intersect around questions of cleaning, monitoring, and failure responses.
  • Describe steps users can take to build robust quality monitoring processes into their decontamination workflow, training, and competencies.

This course is approved to receive 1.0 CE from CBSPD and HSPA.

« » page 1 / 7
Show Buttons
Hide Buttons