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Challenges with ASC Insurance Contracting vs. Out of Network Billing
Stephanie Thomas
60 Min
Product Id: 705676
This webinar will discover the top trends ASC facilities are facing with contracting with Medicare and third party payers. You will get the tips and tricks to ensure your negotiations are successful. You will learn to weigh the pros and cons of contracting to decide if out-of-network billing may be the best route for your business.
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Three Key Risk Assessments in Your ERM Program - ERM, IT, and Internal Controls
Marci Malzahn
90 Min
Product Id: 705777
This risk assessment webinar will discuss how to do perform risk assessments for ERM, IT and Internal control function of your organization. Attendees will learn how to create/develop risk assessments, how to complete the ERM Risk Assessment using the ERM Risk Assessment Matrix. And how to complete the general IT Risk Assessment as well as a thorough Risk Assessment for your Internal Controls.
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Stunning Changes in FDA's Software Regulation
Casper Uldriks
60 Min
Product Id: 705820
This webinar will highlight the changing circumstances with respect to software regulations and FDA’s approach from a regulation to voluntary standard. How to understand the qualifications and terms of participation to clear its software for marketing, what to do in case of cybersecurity intrusion and how to update regulatory program as mobile apps are removed from FDA’s regulatory oversight.
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EU General Data Protection Regulation (GDPR): Compliance for Clinical Trials and Drug Development
Laura Brown
90 Min
Product Id: 705850
This webinar will discuss the new GDPR regulation requirements in the context of clinical trial data, how it applies to clinical trials and pharma industry, the personal data types including clinical trial data, what are the rights of clinical trials subjects, data access requests, informed consent, how to transfer clinical trial data outside EU, data breach reporting, penalties and how to put a data governance program and process to comply with GDPR regulations.
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BREXIT – What's Changing for Life Science Product License Holders/Manufacturers and What You Need to Do Right Now?
Robert J Russell
90 Min
Product Id: 705811
This webinar will discuss how to accurately assess the impact of Brexit up on your operations and existing licensed life products in the UK and EU. How to plan to becoming compliant on “what is known” and how to be agile as the rest of implications become clearer. Impact on Filing Registrations with EMA in Q1 2019, How Will the UK’s Withdrawal Effect the Sunset Clause.
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Safe Use of Ladders and Proper Climbing Practices; Fall Protection on Aerial Lifts; Proper Use of Staging
John J Meola
90 Min
Product Id: 705493
This webinar will review the best practices associated with use of ladders of all types, including the selection, inspection, storage and transport of ladders, along with safe practice when erecting, climbing, working from and descending a ladder. It will also discuss the process and practices related with aerial lifts and working from buckets on an extended boom.
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Proposed NACHA Operating Rules - Hear the Latest NEWS in the Rules Space
Donna K Olheiser
60 Min
Product Id: 705835
This NACHA Operating Rules training session will provide the details on the proposed changes that potentially may be happening in the future. How it is going to impact you and what can you do about it.
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How to Effectively Manage a Construction Project
Keith Warwick
90 Min
Product Id: 704858
This webinar training will explain the process to effectively manage construction projects. The Instructor will discuss reviews of plans and specification, inspection program, order of operations, identification of hazards and safety controls.
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ICD-10-CM Official Guidelines for Coding and Reporting - FY 2019
Pamela Joslin
60 Min
Product Id: 705826
This webinar will discuss overviews of each of the four sections of 2019 ICD-10-CM Guidelines for Coding and Reporting. These are the guidelines that payers use when processing your claims. It will teach how accurate ICD-10 reporting ties to patient encounter, reimbursement and reporting, how to use chapter 7, how to use the A, D, S & documentation requirements. Expert will give examples of commonly used guidelines, such as sequencing, code first, code also, etiology and manifestation.
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Medical Devices: Navigating FDA Requirements for Non-US Organizations
Jonathan Lee
90 Min
Product Id: 705823
This webinar will give an understanding of various processes and compliance requirements for US market entry by non-US medical device manufacturer. It will teach how to comply with pre-market requirements, how to get submission & product clearance/approval, what are various activities to be done post market entry of products (surveillance, reporting, audit, correction & removal).
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Payment System Policy: FFIEC, Risk Management and Fraud Control
Ray Graber
90 Min
Product Id: 705810
This webinar is designed to provide understanding of payment system risk policy, how to do risk assessment and mitigate risk, what can be an optimal organizational structure to manage payment strategy.
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How to Deal with Toxic Behaviours in Healthcare to Improve Patient Safety and Team Performance
Dr. Mitchell Kusy
60 Min
Product Id: 705840
In this Webinar you will learn how to find out toxic people those reduces patient safety, what is their modus operandi, and how to deal with them in terms of feedback, proactive and reactive strategies so that there is improvement of patient safety & team performance. How to spot such people and avoid hiring them.
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FMLA Abuse: How to Identify, Investigate, Deny, and Terminate
Vanessa G Nelson
60 Min
Product Id: 703671
This webinar will assist employers with effective strategies to identify, investigate, and terminate FMLA abusers. Additionally, the course will also instruct employers on when it is appropriate to deny FMLA requests in accordance with the law.
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How to Conduct an ASTM E 2018 Compliant Property Condition Assessment
Keith Warwick
60 Min
Product Id: 705369
Learn how to conduct a property condition assessment (PCA), schedule the field work, conduct the field work, and write the final report. The course will present techniques for developing cost estimates within a reasonable time frame. It will also discuss each of the components of ASTM E 2018 - 15 Standard Guide for Property Condition Assessments.
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Transfer of Analytical Methods According to the USP Chapter <1224>
Dr. Ludwig Huber
75 Min
Product Id: 701971
This webinar will explain the final version of USP Chapter <1224> and FDA guidance for conducting and documenting method transfer between laboratories and sites, and provide tools for effective implementation.
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Microsoft Excel: Using What-If Analysis-When, Why, and How
David H Ringstrom
90 Min
Product Id: 704929
This webinar will discuss the excel What-If Analysis tools within Microsoft Excel’s Data menu. In addition, it will explain Excel Scenario Manager, Data Table features, Excel’s Goal Seek feature, Excel Solver feature, FORECAST and more. Participants can avoid replicating worksheets. The advance functions can also help in comparing different scenario and extrapolate trends based on existing data in your spreadsheets.
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How to Structure and Write a Job Hazard Analysis / Activity Hazard Analysis (JHA – AHA) in Accordance with OSHA 1926 – EM 385
John J Meola
90 Min
Product Id: 705500
This webinar will explore the common failures associated with organizing and writing Job Hazard Analysis / Activity Hazard Analysis (JHA – AHA) documents. It will also de-mystify some of the language and concepts in the traditional JHA process, namely the risk assessment calculator.
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Trial Registration and Results Reporting on ClinicalTrials.gov
Marina Malikova
60 Min
Product Id: 705821
This session will explore the challenges clinical teams and sponsoring organization face in determining if a clinical trials is qualified and required to be registered, determining time frame for updates to be posted and reporting the results. It will explain HHS Final Rule and NIH Policy on Registration/Reporting in ClinicalTrials.gov and provide the steps to registration process in clinicaltrials.gov site.
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The Role of Audit in CECL Compliance
Daniel Clark
60 Min
Product Id: 705528
In this webinar participants will learn what Internal Audit can or cannot do and how the internal auditors can assist in ensuring that CECL processes are robust and complaint with regulator expectations. Attendees will also learn the best ways to leverage an internal audit department as the organization becomes CECL compliant.
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External GMP Audits for Pharma Companies
Ronald Torlini
60 Min
Product Id: 705761
This GMP audit webinar will discuss the importance of external GMP audit, FDA requirements, best practices and steps for external audit execution, reporting, follow up and quality agreements between company and its suppliers/contractors.