Compliance Training Webinars for Regulated Industries

This 90-minute webinar will help you gain an understanding of the regulatory background and provide complete guidance starting from the planning and writing requirement specifications to vendor evaluation, installation and operational qualification and continued testing while in routine use. The webinar also covers the instrument qualification and system validation processes.

In this webinar attendees will learn the GLP requirements for records archiving, discuss common errors many companies make when archiving GLP record, the options for archiving electronic and manual records, and how archiving practices may impact an audit. Also attendees will receive tips on proactive steps they can take to avoid common pit falls and how records readiness can facilitate a smooth audit process.

This webinar will explain how to select an effective Chief Compliance Officer (CCO) or Chief Risk Officer (CRO) best suited to the position. It will also review the skills needed to communicate the essence and structure behind a good compliance program.

This CMS QAPI standards webinar is designed to help surveyors assess compliance with the hospital CoPs for QAPI(Quality Assessment and Performance Improvement). This worksheet is used by State and Federal surveyors on all survey activity in hospitals when assessing compliance with the QAPI standards including validation and certification surveys.

This webinar will discuss various container closure systems that are available for use with liquids and lyophilized products, the components that constitute a container closure system and also cover specialized delivery systems.

In this HR compliance webinar attendees will learn the behaviors, consequences and myths about workplace bullying & how to develop an effective strategies for dealing with workplace bullying and steps to eliminate workplace bullying for building a healthy workplace where employees can thrive.

This training program will provide guidance in recognizing, investigating and reporting suspicious activities. It will also discuss instructions on implementing and maintaining an enterprise wide compliance program to safeguard the financial system from illicit use and combat money laundering and promote national security through the collection, analysis, and dissemination of financial intelligence to the regulatory authorities.

In this Risk Management webinar attendees will learn the risk management guidance on third-party relationships provided by the OCC Bulletin 2013-29 and how the banks continue to increase the number and complexity of relationships with both foreign and domestic third parties such as outsourcing entire bank functions, outsourcing lines of business or products, single third party to perform multiple activities, address deficiencies and engage directly with customers.

This training program will explain the rationale, the legal requirements and some methods commonly used for reprocessing and validating reusable medical devices.

This Healthcare webinar will explore the complications and requirements of each of the rules controlling student health information, HIPAA, FERPA, and 42 CFR Part 2, and provide insights into how to apply the rules in an education setting.

In this Risk Intelligence webinar attendees will learn how to establish and run a successful risk intelligence program in their organization and how to implement the risk intelligence throughout the organization that will lead to a competitive advantage.

This webinar will discuss how the lab payment cuts imposed by PAMA is shifting the competitive landscape for the U.S. laboratory industry. Specifically, the program will cover how the fallout from PAMA is altering the competitive dynamics between national and hospital outreach labs as well as providing a financial advantage to certain speciality labs offering proprietary tests and other labs performing advanced diagnostic laboratory tests (ADLTs).

In this HR compliance webinar attendees will learn the risks of using independent contractors—beyond those associated with worker misclassification and how to avoid or minimize them so that your company and the contractors can enjoy a mutually beneficial business relationship.

In this Healthcare webinar attendees will learn the patient infection risk that is associated with contaminated mobile electronic devices used by healthcare workers. Also attendees will learn the current and novel risk mitigation strategies and a standard method for disinfection of mobile electronic devices.

In this Pharmaceutical Quality Risk Management webinar attendees will come away with the ability to recognize the purpose and value of Quality Risk Management QRM, the level of risk based on severity, occurrence, detectability and how the QRM process is used to make decisions. Also attendees will be able to identify key QRM terminology and recognize the four (4) key components of Quality Risk Management. Finally they will have a strong understanding of the key concepts associated with the risk management risk tools and their application.

This case management webinar will assist the case management department leader(s) in identifying required elements of compliance that must be measured. Critical compliance metrics which must be audited and reported to the appropriate staff member or group(s) will be identified. Not only will the focus on auditing compliance metrics be reviewed, but best practice processes to improve less than optimal outcomes will be discussed.

The webinar training will cover FDA regulations for marketing cosmetics and help attendees learn about new proposed legislation which will place new requirements on cosmetic product marketing in the U.S.

In this supplier management webinar attendees will learn the practical risk-based approaches to selecting, qualifying, and managing your business’ suppliers of all types. Also attendees will learn how to establish a PDCA-based supplier management process.

The ability to construct and present a winning argument by those without direct control over business processes or organizations is the key requirement to excel in today’s risk and auditing environment. This webinar will provide participants with tools and strategies that will improve the quality of your argument thereby improving your chances for providing positive, substantial and effective advice.

In this webinar attendees will learn which products qualify for submissions under section 505(b)(2) of the Federal Food, Drug and Cosmetic Act (FD & C) and the requirements for studies, reference information, and marketing requirements to take advantage of this great sponsorship opportunity.