Compliance Training Webinars for Regulated Industries

This sexual harassment investigation webinar will teach how to conduct harassment and bullying investigations. Attendees will learn legal issues of investigations, characteristics of an investigator, report writing, presentation, communication with case studies and examples.

In this trade compliance webinar attendees will learn the benefits, processes, objectives and implementation of "New NAFTA" or "USMCA" agreement. It will cover the biggest changes in agricultural, manufactured products, labor conditions, digital trades area and how to qualify your products, certifications, and filings.

You may find out after seven or more months of waiting that the 510K has been denied because the software portion of the submittal is inadequate and not compliant. Don’t let that happen. This webinar will teach you how to submit compliant and adequate software enabled medical Devices or Software as a Medical Device to the FDA for 510K approval. Also, learn how to avoid the potential audit risk which might prevent you from selling the approved product if you have been found to not have an IEC62304 Compliant Software Quality System.

This advanced interviewing techniques webinar will teach how to recruit high quality resources through 9 step process to decrease cost, turnover and increase output.

This Medical Device Security webinar will focus on industry leading practices to assist healthcare delivery organizations (HDOs) with the integration of security into medical device procurement to inform procurement decisions, contractual requirements, and compensating controls. Also attendees will learn the required steps involved in the procurement process, some of which include vendor-level and product-level assessments, contractual requirements, and publicly available resources to assist with standardization.

This webinar will discuss the new elemental impurities test requirements as per the new ICH Q3D and USP 232/233 Guidelines, the testing required to comply with it and how to do proper risk assessment and analytical measurements, which drug products are within the scope, the documentation related to control of elemental impurity, which methods required to be validated.

The recent recalls of sartan antihypertensives due to the presence of nitrosamines may suggest increased attention from FDA to toxic impurities in drug products from active pharmaceutical ingredients. The public information about the limits of toxic impurities and about nitrosamines in sartans will be discussed and possible similar situations reviewed in this webinar.

Attend this webinar to learn the best practices for supplier management that will facilitate compliance through the supplier management lifecycle and can help you to manage risk. Also attendees will learn the technology solutions focus on solving supplier management problems, supplier master fraud indicators and compliance requirements for supplier master.

This medical necessity documentation webinar will cover all the key information needed to support your efforts to document and demonstrate Medical Necessity of services.

The webinar will discuss the requirements, the risks, and the issues of the increasing use of mobile devices and texting for patient and provider communications and provide a road map for how to use them safely and effectively, to increase the quality of health care and patient satisfaction. In addition, the session will discuss how to be prepared for the eventuality that there is a breach, so that compliance can be assured.

This Excel spreadsheet compliance training will outline the FDA requirements for Excel spreadsheets used in regulated environments and provide guidance on 21 CFR Part 11 validation.

Learn about the latest CMS hospital CoPs on dietary, food, and nutrition services in this webinar. The program will also discuss the common deficiencies received by hospitals from CMS. Supplementary information about the C&P process for dieticians provided by CMS will be discussed in detail. DNV Healthcare dietary standards will also be detailed.

The annual spending in healthcare now is at $3.5 trillion, and the healthcare industry holds 21% of the U.S. economy. Although the country tops the charts in investments than any other country, the healthcare system delivers average results at best when it comes to affordability, quality, access, and outcomes. Disruption is now emerging from within the healthcare although the efforts to lower costs in the past have fallen short.

In this FDA inspection webinar attendees will learn the basic understanding of Active Pharmaceutical Ingredient Good Manufacturing Practices (ICH Q7) and the most important elements of API GMP to avoid serious deviations and failures during either a Pre-Approval or GMP Inspection.

In this webinar attendees will learn the brazilian labeling requirement for food, cosmetic and probiotics products, Also attendees will gain a complete understanding of claims regulation for food, cosmetic and probiotics according with the local legislation.

This webinar will explore the process increasingly being used by organizations of all sizes to create a safety culture that uses ZERO INCIDENTS as the measure of performance.

The focus of this webinar is to explain the most significant pathogens transmitted on environmental surfaces. The presentation will highlight products and practices for cleaning the healthcare environment, particularly microfiber mops and cloths. It will also detail the benefits of microfiber.

In this webinar attendees will learn the QSR and ISO 13485 requirements for document control and the ideas associated with the development and control of quality documentation. Also attendees will get knowledge on methods and practices that will improve the clarity and control of your document control system. Effective GMP documentation practices will be reviewed to ensure your paperwork is clear, complete, and easy to understand.

This HIPAA Privacy Workforce Training will cover all ongoing activities of a Privacy Program, Notice of Privacy Practices, and workforce expectations. Also this training will provide an overview of HIPAA authorizations, consents, patient’s rights, breach notification, key privacy definitions, penalties for non-compliance and best practices for securing Protected Health Information (PHI). In addition, training will provide an overview of personal representatives and uses and disclosures required by law and safeguarding PHI.

This vendor management webinar will show you how to choose the right vendor, onboarding and set up, manage vendor performance, manage issues and ensure compliance with current FDA regulations and ICH guidelines and have a smooth-running clinical study.