Compliance Training Webinars for Regulated Industries

This webinar is intended for the pharmaceutical industry and associated service providers. It will provide pharmacovigilance and quality assurance departments with an overview of regulatory requirements and expectations for Good Pharmacovigilance Practice audit programmes, with a focus on auditing of activities internal to an organisation as well as those contracted out to service providers and commercial partners, such as distributors and licence partners.

The current coronavirus pandemic has created problems for the management of ongoing clinical trials. In response, regulators have produced guidance aimed at protecting the safety of subjects and clinical trial integrity. This webinar sets out how the US FDA and UK MHRA expect those involved in the management of clinical trials to address these problems.

Attend this webinar to learn how to understand control charts and their underlying statistics, how to choose variables to monitor, how to maintain the records and to plan adjustments. There will be examples and walkthroughs of control chart implementation and use. A review of the relevant statistics will also be done.

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 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.

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.

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 webinar is designed to train managers and HR professionals in how to conduct a thorough and impartial workplace investigation. You will learn how to conduct an investigation keeping it neutral, comprehensive and fair.