Compliance Training Webinars for Regulated Industries

This webinar will include discussions on the risk data aggregation capabilities and internal risk-reporting practices (the Principles) that enhance risk management and decision making processes at financial institutions.

This Analytical Instrument Qualification training will guide you through Understanding of draft for analytical instrument qualification - Essential steps and recommendations for firmware and software validation.

This webinar on Retaliation Claims will help you understand the nature of retaliation in the workplace, What happens when an employee complaints of discrimination or harassment alleges illegal or unethical behavior within your organization? Employees who do so are legally protected from retaliatory action by employers. While the EEOC (and its state counterparts) continues to receive discrimination charges, retaliation claims are the #1 charge

This webinar on Contamination Control will discuss, how the micro lab can be more effectively utilized to prevent or head off microbial contamination issues as well as effectively resolve problems like recurring micro failures, investigations, and ineffective CAPAs.

This session will walk through the basics of UBI and the common sources of it. After laying the groundwork of the three-prong test, we’ll cover the exceptions, exclusions, and what the organization can do to minimize the tax paid from this income.

The session will include discussion of preparing for a cyber attack, preventing and limiting the damage from cyber attacks, being prepared with backups and contingency plans, responding to the attack, and recovering after the attack has been brought under control. Also included is a discussion of how cyber attacks relate to breaches that may be reportable under HIPAA, and how such attacks should be evaluated under the rules.

This Post-market Surveillance (PMS) webinar will discuss in detail the clinical evaluation and risk management requirements as described in MedDev 2.7/1 Rev. 4, EN ISO 14971:2012 and EN ISO 14971:2012 standards and how they are related. It will also explain some of the recent changes in EU medical device regulations.

Reliability methods such as Process Reliability Modeling (PRM) is a very sensitive measurement instrument used to identify areas of medical processes contributing to employee or patient dissatisfaction and loss of revenue. This webinar will discuss the proactive methods such as Process Reliability Modeling will result in processes that are effective, efficient and reliable.

This webinar examines the issues in audit sampling and provides the answers one need to plan audit. It will help attendees understand the use of standard sampling plans in an audit including FDA’s QSIT sampling plans.

If your hospital wants to reduce its rate of denials using a strategic approach, this program is for you. Understanding denials in a comprehensive way will positively affect your practice as a case manager or a case management leader.

This course will arm you with the right tools to conduct a sound investigation, enabling and empowering all involved to focus on the job at hand instead of the problems afoot. Appropriately responding to a complaint of discrimination, harassment or retaliation- or any other workplace issue- can mean the difference between a harmonious work environment and a turbulent one; between a lawsuit being filed and not being filed. A prompt and effective investigation of a workplace problem can curtail and prevent it from growing out of control, rather than escalating from inattention.

This webinar on addressing fungal and bacterial spore outbreaks will discuss case studies on excursion investigations and show how facility design, personnel practices and cleaning and disinfection effect excursion investigations.

This presentation reviews the employment laws that relate to LGBT workers, identifies emerging and unresolved issues, and provides practical pointers for employers concerned with compliance, inclusion, and creation of a respectful workplace environment.

This webinar will explore the multitude of communication channels linking us with our patients and the dazzling array of communication technologies available to us. We will walk through a typical patient experience and map all the communication touch-points. In this session we will do some ‘value stream mapping’ to see how our patient communications can be more effective. Finally, we’ll envision a better future for patient communications.

This webinar on sterility or bioburden test for medical devices will discuss about the various items that should be investigated to determine the root cause, when a failure occurs during a sterility test, and the follow up to the investigation.

This webinar training will detail the purpose and coverage of the Older Workers Benefit Protection Act (OWBPA). It will also highlight the penalties for failure to comply and offer practical pointers for compliance.

This training program will focus on different aspects of a behavior based safety system (BBS), its benefits, coaching workers on safer behavior, measuring BBS success and shortcomings, and more.

This webinar will cover the agency's current enforcement climate for NBFIs, provide detail on recent enforcement actions against MSBs including money transmitters, virtual currency exchanges, and individuals; and discuss FinCEN’s use of GTOs. This webinar will also provide lessons learned and key themes drawn from FinCEN's increase in enforcement actions against NBFIs and its use of GTOs.

This training on fraud investigation will explain how to deal effectively with allegations of fraud and how to conduct internal investigations. It will provide the attendees tips on how to gather evidence in a fraud investigation.

This webinar will teach you what is expected under the new requirements of the Food Safety Modernization Act. Every food company that manufactures or supplies food under FDA jurisdiction is now or will be required to have a Foreign Supplier Verification Program in place.