Compliance Training Webinars for Regulated Industries

This webinar will outline step by step, tools, techniques and actions you can implement the very next day. Even the very first steps you implement will have a surprising impact on your team and you as a leader. This will be your playbook for leadership agility and setting the example for teams.

This webinar will discuss the multi-faceted aspects of bringing a medical device to market. The webinar explores topics ranging from market concept to post-market surveillance. Entering a medical device market involves more than engineering and regulatory compliance. Companies need to consider a variety of issues to successfully enter the medical device market.

No sector has more complex data management and analytical needs than HR. Attend this webinar to learn how AI technology can enhance your department’s ability to gather and process data and make preliminary forecasts based on changing conditions.

This webinar will explore the importance of virus risk management. Food producers and risk managers must be aware of the potential for outbreaks. In the event of an outbreak, they should understand the need for complete cooperation with investigators in an effort to identify effective corrective actions and reduce the public health impact of the event.

This training program will examine LGBT perceptions and stereotypes and help understand the business case for LGBT inclusion in the workforce. It will also establish gender transition guidelines and list organization best practices to minimize discrimination.

This webinar will discuss the emergence, lifecycle, biology, transmission, epidemiology, countermeasures of COVID-19. Countermeasures will be broken down into potential treatments that block the viral lifecycle (monoclonal antibodies, Camostat mesylate, chloroquine/hydroxychloroquine, lopinavir-ritonavir, remdesivir); potential anti-inflammatories (corticosteroids and baricitinib); and immune boosters. Testing methodologies will be covered (RT-PCR and ELISA-based). The development path and progress of vaccines will also be covered.

This webinar is designed to go beyond the basic training to prevent harassment offered through Illumeo and elsewhere. It will talk about some touchy and probably not exactly politically correct ideas in a desire to provide a full understanding of what is happening today and what can be – and should be – prevented in the future.

FDCPA has long been important for financial institutions. With an added focus on consumer rights by activists and now by regulators like the CFPB, it may be time to reacquaint ourselves with this regulation and what we can and cannot do when collecting debts owed us. While changes to the law remain in flux given the current administration’s desire to reduce regulations, the basics are still viable and relevant.

Sampling and sample preparation are both potential sources of variability and bias in analytical chemistry. The purpose of this webinar is to describe a scientifically-sound approach to sampling different types of analytical matrix (including liquids, gases and solids such as powder blends and tablets) and to describe the options available for sample extraction, clean-up and pre-concentration. The webinar would be useful for scientists developing analytical methods or writing sampling plans.

This webinar is designed to help any company avoid ugly accidents and surprises, both minor and massive (e.g., the Deepwater Horizon, the Columbia and Challenger space shuttle disasters). Rather than waiting for an accident to inform them of problems at the workface, it is critical for managers to proactively learn the reality of their workspaces – before an accident occurs. This understanding won’t happen from behind a desk but requires partnering with those actually performing the work to reduce potentially painful surprises and promote continuous improvement.

Attend this webinar to learn about the new EU legal requirements for exporting medical devices to the EU. Learn how to prepare for this MDR requirement and include options for selling your device in the EU and the U.S.

This training program will provide the regulatory requirements (US) for complaint handling in the medical device and pharmaceutical industries. The course will touch on complaint sources, and details will be furnished on the interrelationships regarding complaint handling/change control/adverse event reporting/and recalls. The course will also include timeline requirements associated to adverse event reporting, which reporting formats to use, when to recall and types of recalls.

This webinar will discuss how to properly handle NIOSH listed drugs as per USP <800> requirements from receiving to disposal, including storage, dispensing, manipulation and compounding. Including the proper PPE, deactivation/decontamination required for each handling process.

Too often we find ourselves overwhelmed and frustrated ... not knowing where to turn or what to do. We find ourselves replaying can incident - or the whole day - on our way home from work. Then more replays when we get home - we're stressed and exhausted. We want to be able to get our work done, have good relationships with our co-workers and be able to go home and relax. This webinar will show you how to protect yourself from the painfully obvious toxicity and identify the very subtle toxicity in its infancy. You'll learn key tips, tools and techniques to respond to almost any situation. You’ll go from overwhelmed and feeling helpless to empowerment.

In this webinar you will learn the definition of Leadership Presence. You will learn the seven success skills needed to improve Leadership Presence. If your promotion and career movement have been “stuck” and you are not sure how to improve your chances, you need to attend this webinar.

This webinar will discuss the causes for failure in our deviation systems and recommendations to successfully take a different approach that results in problems finally being solved.

This webinar will demonstrate methodologies for obtaining competitor information to use for the establishment of equivalence. You will also learn how to monitor changes in the global regulatory medical device landscape.

Attend this webinar to explore the importance of Foreign supplier verification program. The FSVP rule requires that importers perform certain risk-based activities to verify that food imported into the United States has been produced in a manner that meets U.S. safety standards and is not adulterated or misbranded with respect to allergen labelling.

Attend this webinar to understand how the COVID-19 pandemic can affect manufacturing operations, employee safety and how to be flexible and creative in these uncertain times when it comes to business continuity.

This training on bio-analytical methods validation will help you to understand the FDA and EMA guidance for Instrumental, ligand binding and cell-based assays and also review of recent 483s impacting validation.