Past CE Webinars
Endoscope Processing “Aha Moments” What Recent Focused Assessments Are Still Telling Us About Endoscopy Reprocessing
Endoscopy teams are working hard to meet evolving expectations for safe, defensible reprocessing, yet assessments of endoscope processing areas continue to reveal the same recurring gaps. In this webinar, we will share practical “aha moments” drawn from recent endoscopy focused assessments in hospital endoscopy departments. For each theme, we will pair what current standards and guidelines expect with what is actually being observed in the field and then translate that gap into actionable, realistic solutions.
Device Integrity Matters: Inspection & Functionality Testing of Shaver Handpieces, Rigid Endoscopes, & Light Cables
Shaver handpieces, rigid endoscopes, and light cables are critical surgical devices that require thorough inspection and functional testing to ensure device performance, patient safety, and compliance with manufacturer Instructions for Use (IFU) and applicable standards. Failures in inspection or functional performance can lead to compromised visualization, device malfunction, delayed procedures, and increased risk to patients and staff.
This session will explore the role of inspection and functionality testing throughout the device life cycle, with emphasis on identifying damage, wear, and operational performance deficiencies that may not be apparent during routine processing. Attendees will review current recommendations, standards, safety alerts, and manufacturer guidance related to these device types, and how they translate into practical workflows within Sterile Processing, the Operating Room, and Biomedical departments.
In addition, recent studies and published data highlighting the impact of routine inspection and functionality testing on device performance, longevity, and risk reduction will be discussed. Participants will gain actionable insights to strengthen quality assurance programs, support compliance efforts, and promote interdisciplinary collaboration to ensure safe and reliable surgical instrumentation.
Endoscope Reprocessing: Ask Us Anything! Live Q&A With the Experts
In this one-hour open Q&A session, our clinical experts will answer real-world questions about standardss, guidelines, troubleshooting, storage, drying, quality monitoring, and more.
Webinar Rewind - Open Wide: Why You Need to Keep Your Instruments Open
This webinar rewind was originally broadcast June 2024. This program will review the importance of keeping various medical devices in the open position during both the cleaning and sterilization process. The attendee will understand which standards, guidelines, and regulations supporting this practice for better patient outcomes. The goal of any medical device reprocessing department is to have clean and functional medical devices. Understanding the importance of keeping medical devices in the open position is one of the fundamentals of that process.
Lint and Particulates in the OR, Are they Really Such a Big Deal?
This webinar will look at lint in the processing and perioperative process and the impact it can have on patient safety.
A Slice of Appreciation: SP Week Ideas
What makes sterile processing so vital in the healthcare experience? And why is acknowledging sterile processing during SP Week (October 12 – 18, 2025) so important? In this presentation, Amy DeGraw and Adam Okada will demonstrate why Sterile Processing Week is important, and how we can show our appreciation for these typically undervalued heroes of healthcare throughout the entire year.
Endoscope Reprocessing 2.0: Navigating the Latest Trends and Best Practices
In this engaging one-hour continuing education program, we will delve into the latest developments and emerging trends in endoscope processing. Participants will explore recent outbreaks linked to endoscope reprocessing, review updated guidelines and standards, and discuss best practices to enhance patient safety. By the end of the session, attendees will gain valuable insights into ensuring compliance with the latest standards and improving the overall quality of endoscope reprocessing.
The Overlooked Risk; How A Near-Miss Inspired a Study on Insulation Testing and Patient Safety
This presentation examines the implications of a personal near-miss that catalyzed further investigation into insulation inspection and testing practices. It analyzes the outcomes of two significant studies conducted in 2019 and between 2022 and 2023, which provide critical insights into insulation performance and safety. Additionally, the abstract reviews relevant recommendations and standards that emphasize the necessity of thorough insulation inspections and testing, underscoring their vital role in ensuring a pro-active approach in employee and patient safety.
Verification in Testing and Inspection for Shaver Handpieces: Case Study 2023-2024
This study that was published in the Jan/Feb 2025 edition of the PROCESS magazine covers the cleaning and integrity of shaver handpieces, which remains a patient safety concern, despite technological advancements in testing and inspection methods. This 1-year study, conducted from 2023-2024 and involving 28 facilities across 10 states, aims to identify issues related to debris and damage in shaver handpieces, as well as the contributing factors linked to inadequate tools for cleaning, inspection, verification, and education. Additionally, the study will review the documented adverse events related to shaver handpieces in the FDA MAUDE reporting database.
Drying Matters: Preventing Infection Through Proper Endoscope Drying - A Collection of Evidence
An in-depth look at the critical importance of thorough Endoscope drying.
This presentation will explore the dangers linked to residual moisture in flexible endoscopes and the serious consequences that can result. We will examine both established and recent scientific studies that provide evidence of the risks posed by moisture left in scope lumens. Finally, we will identify common obstacles to achieving complete drying and discuss practical strategies to address them.
Ope! You Have Surveyors. What's Next?
In this presentation, we'll hear from Infection Preventionist and former Sterile Processing professional, Katie Belski (BSHCA, CRCST, CHL, CIS), on how rounding can improve processes, the impact of mock surveys, and how to maintain survey readiness.
The Hidden Risk of Build-Up Biofilm in Reprocessed Endoscopes
Understanding a unique form of biofilm within endoscopes as the underpinning cause for the prevalence of endoscope-associated outbreaks.
