CMS Hospital Surgery, Anesthesia, and PACU, Standards
Sue Dill Calloway
120 Min
Product Id: 706105
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.
Calling All Compliance Professionals: Communication Is Not Training and - Vice Versa!
Andrea Falcione,Tricia Cornell
60 Min
Product Id: 705968
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.
Target Assessment, Predictive Toxicology and In Silico Methods In Preclinical Safety Assessment
Bryan Norman
90 Min
Product Id: 706108
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.
Dealing with (and Stopping) Overtime Abuse
Janette Levey Frisch
90 Min
Product Id: 706051
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.
The Food Safety Modernization Act (FSMA) Compared to the Global Food Safety Initiative (GFSI) Schemes: Do I Really Have to Do This?
Lisa Petro
90 Min
Product Id: 705955
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.
CFR42 Part 2 – Background and Latest Developments
Chris Hobson
60 Min
Product Id: 706103
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.)
Determining Excreted Drug Dangers under USP 800
Jim Mullowney
60 Min
Product Id: 706096
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.
Mastering the Power of Sensitivity Tools in Financial Modeling
Miles Hutchinson
90 Min
Product Id: 706046
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.
Coatings in Medical Devices – ISO 17327
Gary Fischman
60 Min
Product Id: 706059
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.
Record Retention and Destruction Compliance
David Sanders
90 Min
Product Id: 704445
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.
Veterinary Pharmacy Law: New Regulatory Update
Bernadette Alisantosa
60 Min
Product Id: 705609
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.
Use of Wearable Devices in Clinical Trials
Barry Peterson
60 Min
Product Id: 706061
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.
Coding Concepts – in depth
Jeffrey Restuccio
90 Min
Product Id: 706087
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.
Implementing a GxP Quality Management System
William D Fox
90 Min
Product Id: 706079
This 90-minute GxP Quality Management System webinar introduces you to the planning and implementation of a QMS using a pharmaceutical QMS as a working model and focuses on fundamental concepts of quality, managing quality, systems, processes, managing change and assessment tools.
Scale-Up, Cycle Transfer, and Maximum Throughput Capability for Lyophilized Products
J. Jeff Schwegman
90 Min
Product Id: 702893
This training on lyophilization cycles will cover the process of transferring and or scaling-up a lyophilization process to a larger or different freeze-dryer. It will discuss a methodical approach to understand the thermal properties of a product and simplify the scale-up or transfer process resulting in a consistent product being produced in any freeze-dryer.
What every Manager needs to know about the Risk Intelligence
MaryAnn Lawrence
120 Min
Product Id: 706000
This webinar will help attendees to prepare for a high level understanding of risk intelligence system. Attendees will understand the different risks their organization facing and how to report the risks. This training will help how to implement and communicate GRC to the entire organization.
In-House or Out House, A Corporate Dilemma
Michael Brodsky
60 Min
Product Id: 706084
This session will address factors that food companies need to consider before making decisions on outsourcing analytical food testing or retaining an in-house laboratory and the pros and cons of each approach.
Quality Management System - Structure and Development
Susanne Manz
90 Min
Product Id: 706098
This webinar will help you to develop a Quality Management System (QMS) for Medical Device Companies. An effective QMS sends a message to the FDA and other regulators that your QMS is complete, accurate, and consistently followed. More importantly, it ensures that your personnel can consistently and accurately meet requirements resulting in correct outcomes and quality work.
Thirty Coding, Billing, And Auditing Gray Areas
Jeffrey Restuccio
60 Min
Product Id: 706082
In this webinar, learn the numerous gray areas in billing, coding and auditing. Get recommendations on how to treat every issue and make it a part of your auditing and compliance plan.
Vendor Qualification - How to Design and Implement an Efficient and Compliant Vendor Program
Todd Graham
60 Min
Product Id: 703066
This webinar will tell you what you need to know to design a compliant vendor program, implement it throughout the organization, manage the necessary documentation and effectively communicate with vendors your requirements, needs and issues.







