Compliance Training Webinars for Regulated Industries

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.

In this Harassment Prevention webinar attendees will learn the subtleties of sexual harassment, identifying the risks of allowing negative behaviors and the steps for creating a culture that does not tolerate harassment or bullying. Also attendees will discover a simple tool for coaching those engaging in any behavior that goes against your core values.

In this FDA Inspection webinar attendees will learn about the FDA inspection process & the effective techniques how you and others behave and interact with FDA inspectors during an FDA Establishment Inspections.

This webinar will focus on requirements for taxation and reporting of employee fringe benefits including transportation fringe benefits, section 132 fringe benefits, meals, clothing, housing and education fringe benefits, and third party sick pay. It will also provide best practices to comply with IRS taxation and reporting requirements.

This HR compliance webinar will teach you a systematic process for developing “emotional self-control”. It will help you approach your life with more discipline and will help you learn how to make better choices.

In this webinar attendees will learn the basic understanding of the regulations listed within 21 CFR Part 820, how to apply regulations into your company documentation, describe the must-have systems required for your QMS, Also attendees will learn how to develop a checklist plan for ensuring all elements of the regulations are incorporated into your QMS, and better understand the scope of what will be needed to meet FDA requirements.

Attend this webinar to learn powerful tips and techniques which you can use for hiring process. You will learn interviewing strategies, questioning techniques, errors to avoid and how to conduct effective candidate interviews.

In this webinar attendees will understand the rules that are required to classify products in the Harmonized Tariff Schedule. Minimize errors in classification and better prepare companies for import/export audits from the government. It will also assist companies who are eligible for free trade agreements, ex. NAFTA, and other agreements, in properly completing Certificates of Origin.

This HR compliance training will prepare employers to conduct an internal I-9 audit and also prepare if ICE Police selects them for an external audit. Also attendees will learn the right way to correct I9 documents and Storage Process, recent focus with the new political administration, how long should I9 documents be retained for active and terminated employees and the new immigration guidelines employers need to be aware.

In this webinar attendees will learn the basics of Anti-Dumping (AD) and Countervailing Duties (CVD) Law, Process, Petitions, Filing, and Chronology of Events. Also attendees will learn about involvement of U.S. Government Departments and Agencies in AD/CVD and how to stay clear of AD/CVD problems.

This training on using the QbD approach to analytical method lifecycle is designed to provide participants with a lifecycle approach to developing and validating analytical methods and comply with compendial requirements. The webinar presenter will use case studies to illustrate each stage in the process.

In this HR compliance webinar attendees will learn the strategies to handle workplace conflicts with confidence and how to drive for harmony, reduced drama, and respectful communication. Also attendees will learn 13 major strategies to manage conflict, 2 models for understanding the dynamics of conflict and 9 hot buttons that can inflame conflict and what to do about it.

This FDA compliant SOPs training will explain how to write, organize, and maintain Standard Operating Procedures (SOPs) and train personnel so that you can ensure FDA compliance in a way that is concise, reproducible and easy to follow.

This training program will highlight key differences between SDTM and ADaM models and process flows. It will also focus on key differences between the seven CDISC classes and on best practices to create Dataset.XML from SAS. Attendees will gain a better understanding of the structure and syntax of ODM-XML files as well.