The Ultimate Webinar Directory Curated Across Every Industry and Topic

Financial hardship was the second — highest rated factor swaying a student’s decision to drop out according to a Higher Ed Dive studioID survey on student success priorities and best practices. Getting behind on tuition payments was another major warning sign for at — risk students.Clearly, institutions need to help students better manage campus finances. Technology is key to identifying opportunities that increase student success.In this session, you will discover how to empower staff across your entire campus to better support students with a one-stop view of their financial footprint. Denise Chilston, Manager, of Pima County Community College District, will share specific use cases illustrating how TouchNet’s Student Account Advisor facilitates proactive student support across campus. You will learn how to exceed student expectations for payment types, streamline operations, enable informed conversations that resolve issues and identify intervention opportunities to support student success.Learning objectives:• Understand how your office and students both benefit from a centralized view of the student account• Explore how a holistic dashboard leads to proactive student support• Learn how to simplify processes for every campus office that regularly interacts with studentsDon’t miss this exclusive opportunity to explore the benefits of a centralized view of the student account.Our Speakers:• Jerod Stanton, Senior Manager, Sales Engineering, TouchNet• Denise Chilston, Manager, Pima County Community College District

Companies today often lack a centralized regulatory compliance function and are plagued by fragmented solutions and information silos. With constant changes occurring across the global regulatory landscape, organizations are beginning to adopt tech-enabled solutions to better comply with these obligations. Learn how an end-to-end regulatory compliance solution integrated into GRC processes is transforming how companies approach compliance.Learning Objectives:Recognize regulatory compliance challenges faced by organizations.Use key questions to evaluate the maturity of your compliance program.Discuss how AI and other technology enablers are changing the game on regulatory compliance solutions.Apply best practices for optimizing your regulatory compliance function.CPE Credit(s): 1Field of Study: Information TechnologyInstructional Delivery Method: Group Internet BasedLevel: BasicPrerequisite: NoneAdvanced Preparation: None

A lunchtime webinar for rural and regional practices (MMM2-7).Rural Doctors Network (RDN) invites practice managers and owners to a not-to-be-missed lunchtime webinar focused on the upcoming changes to Medicare Bulk Billing and the new Bulk Billing Incentive Program. The webinar will be tailored to rural and remote practices (MMM2-7).Join Chris Smeed, CEO of Cubiko, for a 45-minute interactive session exploring what these changes mean for your practice. Learn how to interpret key data, understand eligibility, and identify how your practice can benefit.There will be plenty of time for questions, and the session will be recorded for later viewing on Rural Health Pro.Speaker: Chris SmeedChris Smeed is the founder and CEO of Cubiko, an innovative platform that gives practice operators the data and insights they need to run a great clinic. Chris has seen firsthand the opportunities that can be realised through harnessing the power of practice data, having worked across practice management and practice support roles himself for over a decade.

Maximize the efficiency of your multi-source reconciliations.Join us for a highly-practical webinar sharing experiences of revolutionizing payment flow reconciliations across organizations. Get quickly up to speed on dealing with Klarna, PayPal, Visa, MasterCard, American Express, Shopify, and more.By attending, you'll discover:• Best practices for implementing automated reconciliation processes.• How Adra Matcher can optimize your reconciliation and minimize manual errors.• The ways automation with Adra can save time and resources for your finance team.Don’t miss this opportunity to gain valuable insights and learn how Adra Matcher can remove the burden from your reconciliation process!Event DetailsDate: Tuesday, June 10thEuropean Webinar: 10:00AM BSTNorth American Webinar: 11:00AM EDT | 10:00AM CDT | 09:00AM PTSpeaker: Zeph Vu, Senior Solutions Consultant at Trintech

Join us for an insightful discussion of how Unique Placement Advertising is set to redefine the digital marketing landscape.In our upcoming live webinar on Tuesday, 10 June, from 11:00 am to 11:30 am, George Hawwa will share his expertise on leveraging innovative programmatic advertising strategies to capture audience attention effectively.Don't miss this opportunity to learn more about UPA, a more effective and precise advertising method for businesses of all sizes.Speaker: George Hawwa, Founder and Growth Director of Attention Experts.

This session will provide a comprehensive introduction to the U.S. Food and Drug Administration (FDA), its history, key responsibilities, and how it regulates drugs. Participants will gain insights into the regulatory pathways for drug approval and how the FDA exercises flexibility to support novel treatments. Importantly, this session will highlight ways MPN (myeloproliferative neoplasm) patients and caregivers can actively engage in the regulatory process to ensure their voices are heard. Key Learning Objectives:• Gain an overview of the FDA’s history, responsibilities, and common misconceptions.• Understand the regulatory framework governing drug approvals, including safety and efficacy considerations.• Explore the different regulatory pathways available for drug approvals.• Learn how the FDA applies regulatory flexibility to accommodate innovative treatments.• Discover opportunities for MPN patients and caregivers to contribute to the regulatory decision-making process.Meet our expert speaker: Sarah Wicks is an associate at Hyman, Phelps & McNamara, P.C. where she advises drug and biologics companies on a wide range of FDA regulatory and compliance matters throughout the product development and commercialization process. She helps clients navigate human subject protections, clinical trial conduct, product strategies, and interactions with the FDA. She also provides guidance on advertising, promotion, and labeling, ensuring compliance with FDA regulations, and offers expertise in managing internal investigations, responding to FDA inspection observations, and defending against enforcement actions. A strong advocate for the patient voice in drug development, Sarah is dedicated to incorporating patient perspectives into the regulatory process. She plays a key role in planning externally-led patient-focused drug development meetings and works with patient organizations to organize patient listening sessions and adjunct scientific workshops. Her efforts bridge the gap between regulatory frameworks and the needs of the patient community, ensuring that drug development aligns with patient priorities and experiences. By combining her regulatory knowledge with a commitment to patient-centered approaches, Sarah helps clients navigate the complex landscape of drug development while advocating for meaningful patient engagement.

Ready to cut demand charges at your facility and accelerate the payback period of your next energy storage project?Join Moment Energy's Co-Founder & CPO, Gurmesh Sidhu, and guest speaker Alec Zaine from BC Hydro on June 5th, 10:00 AM - 11:00 AM PDT for strategic insights into the BC Hydro Energy Storage Incentive Program and financial tools available to B.C. businesses.‍We’ll be discussing ways to leverage the incentive program to unlock over 90% of the funding necessary for your next battery energy storage system (BESS) project. Secure your seat for the webinar and register today!‍Meet the speakers!Gurmesh SidhuMoment EnergyCo-Founder & CPOAlec ZaineBC HydroProgram Manager

This course will provide an overview of trademarks, including how to select, register using the new USPTO Trademark Center, and maintain. The course will then discuss a number of recent court decisions relating to trademarks, including the risk of using another’s trademarks in ads, risks of comparing products in ads, failure to function, de minimis use, genericness, surnames, and translations.Topics covered include:Intellectual PropertyLaw PracticeAgenda:Trademark OverviewUnderstand how to define a trademarkSliding scale of trademark strengthWhy register a trademark with the USPTOTrademark ProcessWalk through the trademark processSearch, file, and maintainPossible Pitfalls in the Trademark ProcessFailure to adequately select an enforceable trademarkFailure to meet USPTO requirementsFailure to adhere to the “less is more” principleFailure to maintain or even complete registrationAdvertising IssuesRisk of using another’s trademarks in adsRisks of comparing products in adsCourt DecisionsCourt decisions relating to failure to function, de minimis use, genericness, surnames, and translationsQuestions & Answers (as time permits)Duration of this webinar:60 minutesWhen:Premieres in 9 days | June 05, 2025 10:00 AM PTSpeaker:Kirby Drake, Founder, Kirby Drake Law PLLC.

Over the last years, there has been a growing development and use of liquid embolic agents in IR, enabling the treatment of more complex diseases such as vascular trauma and bleeding, arteriovenous malformations, aneurysms, meningiomas, and subdural hematomas – conditions that otherwise could not be effectively treated with other embolic devices. Despite their increasing prevalence, these agents remain underused or unavailable in some hospitals, limiting treatment options for complex diseases. Liquid embolic agents represent an advancement over traditional mechanical embolic materials, making it crucial for interventional radiologists to be proficient in their use within clinical practice.The webinar will highlight key embolic agents such as sclerosants, Gelfoam, glue, and polymers, delving into their physical properties, indications, technical considerations, efficacy, and the latest innovations.Learning objectives:• To understand the differences between different types of liquid embolic agents and their specific uses.• To learn about the main liquid embolic devices currently in use and their composition.• To understand the clinical applications of liquid embolic devices during elective procedures.• To learn how to use embolic devices during emergency procedures.Programme:Introduction by the moderator - Alessandro Cannavale (Rome/IT)Clinical assessment of patients undergoing embolization procedures - Andreas Mahnken (Marburg/DE)Overview of currently available and upcoming embolic agents - Enrique Esteban Hernandez (Valencia/ES)Sclerosant agents and challenging cases - Lakshmi Ratnam (London/UK)Glue and LIPIODOL and challenging cases - Alberto Alonso-Burgos (Madrid/ES)Polymers and challenging cases - Romaric Loffroy (Dijon/FR)Discussion and Q&ATake home points by the moderator - Carolina Lanza (Milan/IT)FacultyModerators:• Alessandro Cannavale (Rome/IT)• Carolina Lanza (Milan/IT)Speakers:• Alberto Alonso-Burgos (Madrid/ES)• Enrique Esteban Hernandez (Valencia/ES)• Romaric Loffroy (Dijon/FR)• Andreas Mahnken (Marburg/DE)• Lakshmi Ratnam (London/GB)

In a season marked by patchy emergence, lack of moisture and tough calls, this session is about taking stock and not rushing decisions.Barry Mudge, Port Germain (Upper North SA) farmer, will discuss using gross margins to assess the marginal return of continuing seeding or in some cases re-seeding. Calculations and thinking presented by Barry have been conducted as part of the national GRDC-funded RiskWi$e project.Panel discussion:Barry will be joined by Jeff Braun (The Agronomist) and Craig Drum (Dagro Consulting) to dive into examples and regional insights around decision making in regions currently experiencing tough seasonal conditions.Speakers:Jeff Braun, Craig Drum