Compliance Training Webinars for Regulated Industries

This 1-hour webinar will go into the specifics of how materials regulations and compliance with those regulations affect selling products to customers and placing finished goods on markets around the world.

This training program will discuss how to calculate overtime under the FLSA rules for nonexempt employees. The session will also cover definitions of overtime and calculation examples.

Cost effective strategies should be designed to prevent, detect and/or mitigate the impact of potential crises. Reducing system vulnerabilities is typically accomplished by delineating then remediating single as well as combined configuration failure points. In this webinar, get an overview of Business Continuity and what an audit encompasses. It will discuss primary business continuity audit program considerations.

This webinar will discuss key components of requirements and expectations for sponsors conducting nonclinical safety studies at Contract Research Organizations (CRO’s). The webinar will also review Sponsor responsibilities for assessing and auditing CRO’s conducting nonclinical studies on their behalf.

When interviewing candidates or drafting applications, employers must avoid certain questions which could reveal characteristics protected by Title VII of the Civil Rights Act or other laws. If the candidate is ultimately rejected for the position, he or she may claim that the decision was discriminatory based upon the protected characteristic brought up in the interview. This webinar will cover the various topics and questions an interviewer should avoid as well as which questions are permissible to get the information legitimately needed.

This webinar will go over in detail the CMS hospital anesthesia hospital CoPs that all hospitals that accept Medicare patient must follow. The number of deficiencies for the anesthesia tag numbers will be discussed.

In this HR compliance training attendees will learn an effective compliance program reaches both the hearts and the minds of your audience, combining communications and training.

This webinar will discuss current best practices to predict potential safety risks in drug discovery. It will describe how early target assessment and analysis can help identify potential safety risks, allowing researchers to design issue-specific mitigation approaches. It will also describe how predictive toxicology and in silico methods can work together and inform drug discovery optimization campaigns.

In this webinar, you will learn how to stop unnecessary and/or unauthorized overtime to cut tremendous losses, and needless payments for extra hours worked or claimed.

This webinar will focus on how Global Food Safety Initiative (GFSI) food safety standards overlap or contrast with FDA food safety regulations and the different approaches taken by FDA and GFSI standards to ensure the safety of the US food supply.

This webinar will discuss how to navigate, from a compliance perspective, a key Federal privacy law, known as 42 CFR part 2 along with several recent new regulations that all impact on the safe management of Substance Use Disorders (SUD.)

In December of this year, USP 800 will take effect. Each entity that handles Hazardous Drugs (HD’s) must have a designated person who is qualified and trained to be responsible for developing and implementing appropriate procedures overseeing entity compliance with USP 800 and other applicable laws. This course will show you how to determine which of the almost 300 HD’s you need to handle in the same manner in the pharmacy and as they are excreted by the patient. We will look at recommendations from the international Society of oncology pharmacy practitioners (ISOPP) on the list of drugs with excretion times as well as other sources.

This sterilization validation process training webinar will review the FDA or ISO requirements for tests following validation and emphasis is placed on the appropriate tests for validation, the appropriate routine tests and the frequency of testing.

In this financial modeling course, learn how to put the powerful sensitivity tools of Microsoft Excel to work. Learn how to unlock the power of scroll bars and spinners, goal seek, one and two-input data tables and scenario manager in your models. See samples of tools, demonstrations with complete instructions for creating and using each of these tools. Learn the top 20 best practices of solid model design, development and delivery.

This webinar provides an understanding of coating systems in general, differences in how coatings are applied, what their weak points might be and how to assess the properties that are appropriate for their needs. The new document ISO 17327 will be discussed and controversies that form from potential use of that document will be assessed.

This training program will offer attendees an understanding of record schedule defensibility and best practices to take steps toward improvements. The IRS states entities need to be fully informed of the code relating to Record Retention and Destruction to determine what records are necessary to stay in compliance or face fines. According to IRS and state statistics of the entities audited over the past three years, 82% could not supply adequate records to pass an audit - resulting in substantial fines for non-compliance.

This webinar will cover the legal regulations for dispensing and record keeping of controlled substances. This training will discuss the new changes in food animal antimicrobial drugs from OTC to Rx. Compounding guidelines and legal ramifications of dispensing human drugs to animals will be discussed in detail. It will review new drug dosages forms and extra labels use and further it will review what is legal for technicians and what to do when handling medications.

This training program may well change the way in which you prepare or analyze the very next time extension request you have to deal with. It will discuss rules concerning time extension requests, arguments about waiver and apportionment of liquidated damages, concurrent delay issues and who has to prove concurrent delay, and more.

This webinar will provide a basic understanding of how devices work, how to identify quality devices, how to get the most value from the information collected, and how to be well positioned for the growth in this field. The new mobile devices guidelines provided by the Clinical Trials Transformation Initiative (CTTI, a private/public partnership initiated by Duke University and the FDA) will be reviewed.

This is a comprehensive Coding Concepts course suitable for management and Providers. It is especially useful for non-coders or beginning coders. Many of the topics presented here are “must know” concepts that everyone responsible for coding should know.