Learning Center
INS 2026 Virtual Conference
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Register
- Non-member - $800
- Member - $660
The INS 2026 Virtual Conference is a great option for anyone who can’t join us in person. With 20 curated sessions available virtually and on-demand, CRNI®s can earn up to 40 recertification units (RUs) at their own pace. This year’s virtual lineup includes 3 specialty tracks—Vascular Access Devices, Alternative Care Settings, and Disease States—each designed to strengthen your infusion therapy practice from anywhere.
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Contains 3 Component(s), Includes Credits Includes a Live Web Event on 04/12/2026 at 8:00 AM (EDT)
Vascular access device (VAD) selection is a complex and evolving part of infusion therapy practice. The key foundational concept to VAD selection is vessel health and preservation, selecting the optimal VAD that will support administration of required infusion therapy while maintaining patient safety. It includes 4 basic segments: patient specific assessment and appropriate VAD selection, skilled clinician VAD insertion, VAD management to promote positive outcomes, and analyzing organizational data to identify areas for improvement. The choice of the correct VAD for placement is reliant on thorough understanding of VAD and infusate characteristics within the context of the individual patient’s condition and infusion therapy requirements. This session will review the risks and benefits of VAD options, the infusate components that increase injury risk, then apply those criteria to promote patient safety through to a case-based discussion from various clinical settings.
Vascular access device (VAD) selection is a complex and evolving part of infusion therapy practice. The key foundational concept to VAD selection is vessel health and preservation, selecting the optimal VAD that will support administration of required infusion therapy while maintaining patient safety. It includes 4 basic segments: patient specific assessment and appropriate VAD selection, skilled clinician VAD insertion, VAD management to promote positive outcomes, and analyzing organizational data to identify areas for improvement. The choice of the correct VAD for placement is reliant on thorough understanding of VAD and infusate characteristics within the context of the individual patient’s condition and infusion therapy requirements. This session will review the risks and benefits of VAD options, the infusate components that increase injury risk, then apply those criteria to promote patient safety through to a case-based discussion from various clinical settings.
Learning Objectives: At the conclusion of this session, learners will be able to:
• Describe characteristics of peripheral and central vascular access devices through risk/analysis perspective
• Identify infusate components that increase the risk of patient injury
• Apply VAD and infusate characteristics in a case scenario format to optimize patient safety
Contact Hours: 1
CRNI® RUs: 2
$i++ ?>Barb Nickel, APRN-CNS, CCRN, CRNI®
Barb Nickel, APRN-CNS, CCRN, CRNI®, is a Clinical Nurse Specialist at a large health care system in the United States, responsible for staff development and process improvement to optimize outcomes in multiple areas of clinical practice, including critical care, infusion therapy, sepsis, and new graduate transition to practice. Ms Nickel has presented nationally and published in several peer-reviewed journals on infusion-related topics. She was the Chair of the 2024 INS Infusion Therapy Standards of Practice (SOP)Committee, and is now Chair of the 2027 INS SOP Committee. She also serves as Adjunct Research Fellow for Griffith University, Queensland, Australia.
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Contains 3 Component(s), Includes Credits Includes a Live Web Event on 04/12/2026 at 8:00 AM (EDT)
Intravascular catheters are among the most frequently used medical devices in healthcare. Their widespread use—across millions of insertions, access procedures, and maintenance events—significantly increases the risk of healthcare-associated infections. The purpose of this presentation is to provide a framework that vascular access team (VAT) members can use to reduce the risk of post-insertion infections associated with vascular access devices (VADs). Recent U.S. and international infection prevention (IP) research highlights a growing number of emerging issues and recommended interventions relevant to vascular access teams (VATs). These include hand hygiene adherence, proper use of personal protective equipment, and environmental exposure risks such as contaminated sinks. New federal legislation on hospital-onset bacteremia has expanded prevention efforts to all VADs, not just central lines. Additional focus areas include defining core components of infection risk mitigation, gaining leadership support, and optimizing catheter placement to reduce infection. Advances in antimicrobial dressings, blood culture contamination reduction, and updated IP strategies for peripheral IVs are also emphasized. Finally, monitoring post-insertion care with attention to bundle compliance remains a key priority. A review of emerging IP issues will inform necessary updates to VAD clinical practice protocols. These revisions aim to enhance patient safety by strengthening infection prevention across assessment, insertion, and maintenance practices.
Intravascular catheters are among the most frequently used medical devices in healthcare. Their widespread use—across millions of insertions, access procedures, and maintenance events—significantly increases the risk of healthcare-associated infections.
The purpose of this presentation is to provide a framework that vascular access team (VAT) members can use to reduce the risk of post-insertion infections associated with vascular access devices (VADs). Recent U.S. and international infection prevention (IP) research highlights a growing number of emerging issues and recommended interventions relevant to vascular access teams (VATs). These include hand hygiene adherence, proper use of personal protective equipment, and environmental exposure risks such as contaminated sinks.
New federal legislation on hospital-onset bacteremia has expanded prevention efforts to all VADs, not just central lines. Additional focus areas include defining core components of infection risk mitigation, gaining leadership support, and optimizing catheter placement to reduce infection. Advances in antimicrobial dressings, blood culture contamination reduction, and updated IP strategies for peripheral IVs are also emphasized.
Finally, monitoring post-insertion care with attention to bundle compliance remains a key priority. A review of emerging IP issues will inform necessary updates to VAD clinical practice protocols. These revisions aim to enhance patient safety by strengthening infection prevention across assessment, insertion, and maintenance practices.
Learning Objectives: By the end of this session, participants will be able to:
- Summarize the emerging IP issues that will influence VAD practice.
- Summarize new peer-reviewed studies and expert guideline recommendations that impact VAD practice.
- Reproduce a listing of emerging IP intervention considerations that reflect recent research findings.
Contact Hours: 1
CRNI® RUs: 2
$i++ ?>Robert Garcia, MT(ASCP), CIC, FAPIC
Robert Garcia is an infection preventionist/consultant and has been a member of the Association for Professionals in Infection Control and Epidemiology (APIC) since 1980. In 2016, he was selected as a fellow at the Association for Professionals in Infection Control and Epidemiology (APIC), a designation for experienced IPs who have had significant contributions to the field of infection prevention. He is the certification infection preventionist/director at nine hospitals in New York City and the principal researcher on the effectiveness of silver-hydrogel urinary catheters, chlorhexidine skin antisepsis, and comprehensive oral care. Robert is a current or former member of APIC’s National Strategic Planning Board, Education Committee, and/or CBIC, as well as a trainer for APIC’s EPI Clinical Course. He is a contributor to APIC’s Text of Infection Control and Epidemiology; was a reviewer for the 2005 HICPAC Guidelines on Isolation; and since 2001 has been an editorial board member and/or reviewer for the American Journal of Infection Control, where in 2016 he was ranked among the top 25th percentile of reviewers. He has more than 100 publications and media interviews ranging from institutional costs of infection to prevention of HAIs to environmental contamination to microbiology to reducing occupational exposures.
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Contains 3 Component(s), Includes Credits Includes a Live Web Event on 04/12/2026 at 9:15 AM (EDT)
More information coming soon...
Catheter-associated bloodstream infection (CABSI) prevention has traditionally focused on 2 primary routes: skin flora migration along the catheter (extraluminal) and contamination introduced through the hub (intraluminal). Yet a third pathway—gross “outside-in” contamination from environmental or body fluids—remains underrecognized and largely absent from current infection-prevention (IP) bundles. The “What is Missing” concept addresses this overlooked pathway, taking a closer look at targeted interventions. This session examines the evidence for this neglected route, its clinical consequences, and the procedural vulnerabilities that permit it. This presentation highlights the urgent need to address this gap in protection and will review practical solutions for clinicians in all settings. Integrating these strategies into vascular access practices supports a systems-based approach to improve infection control to close the gap between ideal protocols and real-world practice.
Learning Objectives: At the conclusion of this session, learners will be able to:
- Identify the 3 primary routes of CABSI, including the underrecognized “outside-in” contamination pathway
- Analyze real-world evidence and case data to determine the role of gross environmental contamination in the development of CABSI
- Evaluate the limitations of current infection prevention practices and technologies in addressing visible contamination of vascular access components
- Recommend practical, system-based interventions to reduce the risk of catheter-related infections in clinical practice
Contact Hours: 1
CRNI® RUs: 2
$i++ ?>Nancy Moureau, PhD, RN, CRNI®, CPUI™, VA-BC
Nancy Moureau, PhD, RN, CRNI®, CPUI, VA-BC, is a globally recognized leader and the founder of PICC Excellence, Inc., a premier provider of education on infusion therapy and vascular access device (VAD) insertion and care for over 3 years. Dr Moureau’s extensive clinical experience includes pediatric, neonatal, intensive care unit (ICU) peripherally inserted central catheter (PICC)/IV teams, and home infusion care.
As CEO of PICC Excellence, she leads the development of over 8 online educational courses and pathways, emphasizing insertion competency and evidence-based practices. Her responsibilities include education development, research, global speaking engagements, legal reviews, manufacturer consulting, and active clinical practice for peripheral and central vascular access.
Dr Moureau pioneered PICC Certification™ (CPUI™) and Neonatal PICC Credentialing (CNPI) programs, validating inserters' education and competency. Most recently, she introduced a systematic UGPIV Mastery Learning Process, an ultrasound-guided peripheral insertion toolbox that earned the Infusion Nurses Society’s (INS) Seal of Approval—the first of its kind.
To connect with Dr Moureau, visit www.piccexcellence.com, or email her at nancy@piccexcellence.com.
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Contains 3 Component(s), Includes Credits Includes a Live Web Event on 04/12/2026 at 9:15 AM (EDT)
More information coming soon...
More information coming soon...
Contact Hours: 1
CRNI® RUs: 2$i++ ?>Joan Harvey, DNP, RN-BC, CCRN
Joan Harvey, DNP, RN, BC, CCRN, has extensive experience in Critical Care Nursing and Gerontology. She is board certified in both and currently sits on a panel for the ANCC as a content expert for the Gerontological exam. She is a Professor at Georgian Court University, teaching Generic BSN students. Her passion for safe medication use dates to when she was at the graduate nurse level. She remains focused on quality education regarding safe medication administration.
$i++ ?>Susan H. Weaver, PhD, RN, CRNI®, NEA-BC
Nurse Scientist, Hackensack Meridian Health
Susan Heidenwolf Weaver, PhD, RN, CRNI®, NEA-BC, is a nurse scientist at the Ann May Center for Nursing at Hackensack Meridian Health and the New Jersey Collaborating Center for Nursing. Sue has experience as an ICU nurse and Nurse Educator, with responsibility for teaching the IV Course, Operations Manager and Evening Administrative Supervisor. As a nurse scientist, Sue has conducted research on the nursing workforce, with a focus on the evening and night administrative supervisor role. Sue has presented and has been published on critical “behind the scenes” nurse leadership roles. Sue lives in Lake Mohawk, New Jersey, has 3 great children and is a basket weaver!
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Contains 3 Component(s), Includes Credits Includes a Live Web Event on 04/12/2026 at 10:30 AM (EDT)
Biological drug products—including monoclonal antibodies and protein-based therapeutics—must be administered parenterally and are highly sensitive to environmental stressors such as mechanical agitation, light exposure, and freezing. In addition to these external factors, the materials and devices used during preparation and infusion can also introduce degradation risks due to shear stress or incompatibility. This session explores how formulation scientists anticipate and mitigate such risks during product development and manufacturing scale-up. Drawing from both research and industry experience, the presentation highlights strategies designed to ensure biologics remain stable and effective after leaving the manufacturing site. Insights from a recent nurse-focused survey on biologic handling will also be shared, along with discussion of their potential implications for future product design. The session concludes by identifying nurse-informed opportunities to make biologics more resilient and user-centric.
Biological drug products—including monoclonal antibodies and protein-based therapeutics—must be administered parenterally and are highly sensitive to environmental stressors such as mechanical agitation, light exposure, and freezing. In addition to these external factors, the materials and devices used during preparation and infusion can also introduce degradation risks due to shear stress or incompatibility. This session explores how formulation scientists anticipate and mitigate such risks during product development and manufacturing scale-up. Drawing from both research and industry experience, the presentation highlights strategies designed to ensure biologics remain stable and effective after leaving the manufacturing site. Insights from a recent nurse-focused survey on biologic handling will also be shared, along with discussion of their potential implications for future product design. The session concludes by identifying nurse-informed opportunities to make biologics more resilient and user-centric.
Learning Objectives: By the end of this session, participants will be able to:
- Discuss the sensitivity of biological drug products related to improper handling and administration.
- Recall the proper product handling required to reduce the risk of degradation.
- Describe common nursing practices in the handling and administration of biologics.
Contact Hours: 1
CRNI® RUs: 2
$i++ ?>Ahmad Sediq
Ahmad Sediq, PhD, is a pharmacist with a PhD degree in pharmaceutical technology from Leiden University in the Netherlands. Dr Sediq worked as a formulation scientist at Janssen Vaccines in the Netherlands, where he was responsible for late-stage development and commercial launch of adeno-associated virus- (AAV)-vector-based vaccine products for Ebola and human immunodeficiency virus (HIV). He joined Lonza DPS in 2018, where he was principal scientist and group leader in the Formulation Development group. At Lonza, his team was responsible for early- and late-stage drug product development of various biological formats. In 2022, Dr Sediq joined Roche/Genentech, where he is taking the lead of early- and late-stage drug product design and development for treatment of inflammatory bowel disease and lung cancer.
Dr Sediq is interested in applying his technical and scientific knowledge into pharmaceutical care and treatment. Therefore, he is passionate of performing research at the interface of pharmaceutical technology and clinical practice.
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Contains 3 Component(s), Includes Credits Includes a Live Web Event on 04/12/2026 at 10:30 AM (EDT)
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Contact Hours: 1
CRNI® RUs: 2$i++ ?>
Claudia Orth
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Contains 3 Component(s), Includes Credits Includes a Live Web Event on 04/12/2026 at 2:30 PM (EDT)
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Contact Hours: 1
CRNI® RUs: 2$i++ ?>Jeannine Blake, PhD, RN
Jeannine Blake, PhD, RN, is a nurse scientist with a clinical background in surgical intensive care nursing and a passion for advancing health care innovation using an interdisciplinary nurse-engineer approach. Her research focuses on improving intravenous (IV) pumping technology accuracy, flow steadiness, and usability, with a current interest in understanding the impact of alarm management on nursing time and patient experience. She is dedicated to improving patient outcomes, streamlining nursing workflows, and integrating IV pumps more effectively into real-world clinical practices.
Dr Blake earned her PhD in Nursing Science and completed a Postdoctoral Research Fellowship in Mechanical and Industrial Engineering at the University of Massachusetts Amherst. She is now an Assistant Professor in the Elaine Marieb College of Nursing and is affiliated with the Elaine Marieb Center for Nursing and Engineering Innovation. She continues her research mission in this role to build evidence that informs infusion practices and optimizes nursing workflows.
Dr Blake contributes to the development of global safety standards for infusion therapy as a member of the Association for the Advancement of Medical Instrumentation (AAMI) technical information report (TIR) Infusion Standards Committee and has been an invited clinical advisor to the International Electrotechnical Commission (IEC) Infusion Standards Working Group. For her work in this space, she is the 2025 AAMI Young Professional Award winner.
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Karen Meade
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Contains 3 Component(s), Includes Credits Includes a Live Web Event on 04/12/2026 at 2:30 PM (EDT)
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Contact Hours: 1
CRNI® RUs: 2$i++ ?>Victor D. Rosenthal, MD, PhD
Prof. Victor D. Rosenthal, MD, PhD, is a specialist in Internal Medicine and infectious diseases with an Infection Prevention fellowship at Wisconsin University and a certification in Clinical Effectiveness from Harvard University. He is a Professor in the Public Health Department at the University of Miami.
Since 2002, he has been the Founder and Chief Scientific Officer of the International Nosocomial Infection Control Consortium (INICC), which researches the surveillance and prevention of central line-associated bloodstream infections (CLABSIs) in 45 countries in Latin America, Asia, Africa, the Middle East, and Eastern Europe. In this setting, he has led over 2,500 researchers. Over the last 30 years, he has been a keynote speaker at thousands of events in 900 cities in 71 countries.
He has 421 scientific publications, which have been cited in over 28,500 peer-reviewed papers. His H index is 72. He serves on the editorial boards of the American Journal of Infection Control (AJIC) and other journals, reviews over 100 peer-reviewed journals, including The Lancet, and has received 10 international awards for his research, including those of APIC and the Society for Healthcare Epidemiology of America (SHEA).
He has collaborated as an editor-in-chief or reviewer of standards for several scientific organizations, including the Infusion Nurses Society (INS), International Society of Infectious Diseases (ISID), Association for Vascular Access (AVA), Joint Commission International (JCI), World Health Organization (WHO), and the governments of Hong Kong, Taiwan, Colombia, Brazil, and Argentina. He is the Editor-in-Chief and Committee Member of the INS Infusion Therapy Standards of Practice, to be published in 2027, and the editor-in-chief of the 2024 ISID Guidelines to Prevent CLABSI.
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Contains 3 Component(s), Includes Credits Includes a Live Web Event on 04/13/2026 at 8:00 AM (EDT)
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Contact Hours: 1
CRNI® RUs: 2$i++ ?>
Baudolino Mussa
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Contains 3 Component(s), Includes Credits Includes a Live Web Event on 04/13/2026 at 8:00 AM (EDT)
Peripheral intravenous infiltrations and extravasations (PIVIEs) remain a significant source of preventable harm, patient distress, and healthcare cost, especially in pediatric settings, where families often cite intravenous (IV) starts and failures as the most stressful part of a hospitalization. With over 80% of hospitalized patients requiring a peripheral intravenous catheter (PIVC), proactive prevention strategies are essential. This session introduces and discusses the P.O.K.E. initiative (Previous PIVIE, Oral transition, Keep it, Educate PIV plan to family and team), a structured communication tool designed to reduce PIVIE rates through interdisciplinary collaboration and family engagement.
Peripheral intravenous infiltrations and extravasations (PIVIEs) remain a significant source of preventable harm, patient distress, and healthcare cost, especially in pediatric settings, where families often cite intravenous (IV) starts and failures as the most stressful part of a hospitalization. With over 80% of hospitalized patients requiring a peripheral intravenous catheter (PIVC), proactive prevention strategies are essential. This session introduces and discusses the P.O.K.E. initiative (Previous PIVIE, Oral transition, Keep it, Educate PIV plan to family and team), a structured communication tool designed to reduce PIVIE rates through interdisciplinary collaboration and family engagement.
Learning Objectives: At the conclusion of this session, learners will be able to:
- Understand the complications associated with PIVIE and their impact on the child, the family, and the health care system
- Identify evidence-based tools for the prevention of PIVIE
- Evaluate current PIVIE prevention strategies implemented to determine alignment with evidence-based best practices and identify opportunities for improvement
- Recognize key risk factors that contribute to its occurrence in pediatric patients
Contact Hours: 1
CRNI® RUs: 2
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Julie Marshall
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Jessica Perdue
