Compliance Training Webinars for Regulated Industries

This webinar will review not only the Anti-Kickback Statute and its safe harbors, but will provide an in-depth overview of OIG guidance and advisory opinions dealing with marketing activities, as well as a review of case law regarding marketing behavior.

In this training program attendees will learn whether they are aware on what determines requirements, criteria and decisions in Unemployment Insurance Benefits. There are a couple of factors that dictate whether a former employee will receive unemployment compensation, which are, the circumstances of the employee's departure and whether the employer contests the employee's claim. If a former employee files a claim, you will need to decide whether or not to contest it.

This webinar will address engineering, administrative and PPE measures aimed at eliminating and reducing occupational airborne silica dust exposures and generation, in accordance with the most recent revision to the OSHA silica dust exposure standard. and provide examples of compliance oriented documents, hardware, techniques and training course components.

This HR documentation best practices webinar will discuss what, when and how to document employee’s performance review, what types of documents can be created, the terminologies (subjective vs objective) to use, the best practices of creation and usage in cases of providing effective feedback and manage employee rebuttals. Understand the role of documentation in investigation and lawsuits.

While there are innumerable ways to detect, prevent and investigate embezzlement, it is not always easy to organize a consistently effective anti-embezzlement strategy. This webinar will guide you through the common and not-so-common forms of embezzlement—with uniquely instructional case studies. It will emphasize the red flags of each and go on to highlight best practices in embezzlement risk mitigation.

This analytical method validation webinar will help you understand the various parameters required for a successful method validation. It will highlight various requirements of USP and FDA for a successful method validation. This will be helpful for All pharmaceutical analytical chemists & supervisors responsible for validating new or modified analytical methods, and the personnel responsible for hosting FDA inspections, responding to 483s and Warning Letters or preparing NDAs or ANDAs.

In this webinar attendees will learn the common errors and challenges involving coding and CDI queries and identify whether the coding queries are compliant or not? Also attendees will review coding guidelines, resources from AHIMA and ACIDS, query templates, practice case examples applicable to both outpatient and inpatient settings.

Learn marketing authorization process for health products in Brazil with focus on documentation, approval process, labeling, advertising, post marketing vigilance. Understand the health protection goals of the law; Polices to meet the applicable regulations. Learn how to harmonize your regulatory strategy for getting approval at less time and cost. How the agency ANVISA works.

This 90-minute session will help you to get better understanding of pacing delay and how the issue may be dealt with by both owners and contractors. Instructor will defines the term; identifies what constitutes pacing delay; and sets forth the contractor’s legal right to pace an owner caused delay. He also explains the practical impact of pacing delay, both to the project as well as to a delay claim.

In this webinar attendees will learn the good manufacturing practices required for any medical marijuana production operations related to international and US individual state cannabis regulations to determine how to best operate their cannabis operations.

In this HR webinar attendees will learn how to implement artificial intelligence policies in HR process like (recruitment, performance appraisal, training & planning etc.) and what are the impacts of artificial intelligence on employment numbers commencing 2020 and beyond. You will understand how an integrated AI program works and benefits.

At this webinar you will learn about common billing mistakes which can help you in avoiding costly denials. You will learn how to properly identify trends and prevent denials, pre-authorizations and insurance verifications. It will cover demographics denials, authorization denials, medical necessity denials and out of network etc.

The hallmark of an interactive, data-driven dashboard is the ability to see and understand data at the speed of thought. This training webinar will deliver the skills needed to design well-planned Excel dashboards that present answers to questions in real-time, render visually striking displays, turn insight into action, help accomplish your firm’s objectives and improve your Excel skills. Attendees will be able to define key performance indicators and build a dashboard in Excel to monitor them.

SR Letter 11-7 outlines the regulatory expectations with respect to the risk management processes and internal controls that banks must implement. This training program will detail the purpose and scope of the guidance, and discuss effective model risk management for financial institutions.

This ACH training program will review common consumer issues and situations while handling ACH disputes. It will guide participants in deciding the appropriate course of action in given situations. Participants will also learn what to do when a customer/member won’t complete a WSUD.

This webinar on Cal/OSHA Enforcement and Defenses will cover the recent changes in the law, specifically the four most significant developments in Cal/OSHA enforcement and defense that will have an impact in 2015.

Attend this webinar and learn skill building techniques that include the "do's & don'ts" of loan committee, “reading” the personalities of the committee members, understanding the difference between an “outside” versus “inside” committee member, exploring “group dynamics,” and tips on how to actually make a clear, concise, and motivating presentation.

This workplace electrical safety course will discuss safety requirements in the workplace as per NFPA 70E 2018 Standard for electrical safety . This includes electrical components and work on electrical systems; and how to conduct electrical audits and inspections.

A tougher U.S. FDA expects a company to maintain certain documents in equipment, process and product software V&V. These documentation requirements can assist in a 21 CFR Part 11 CGMP records / signature V&V as well. This training program will provide valuable assistance to all regulated companies in evaluating their existing or anticipated software V&V activities and documentation requirements, especially in light of the changes in the FDA's stance vis a vis industry compliance, past problems, and the growing cloud environment. It will help attendees understand and recognize the most common software V&V failings and their fixes. The webinar will allow attendees to develop and use a repeatable software V&V template for all software validation projects.

This program is going to cover the proposed changes that CMS wants to make for all hospitals including critical access hospitals. These changes will affect many different departments of the hospital including nursing, QAPI, medical records, lab, restraint standards, discrimination, patient rights, and more.