FDA: Mock and Pre-Approval Inspections (PAIs) - Part II
Vanessa Lopez
120 Min
Product Id: 706258
This course for pharmaceutical professionals provides the information they require, to prepare for and understand what will happen during a mock audit and during a Pre-Approval Inspection (PAI).
US Import: How to prepare for a Customs Audit
Deep SenGupta
60 Min
Product Id: 703612
This webinar will explain the structure and timeline of a customs audit, and teach attendees how to successfully prepare for an audit. Attendees will learn the best practices for trade compliance and customs compliance that you can implement while importing/exporting to minimize penalties. Also you will learn how to establish a reasonable care process, identify the characteristic of internal controls along-with real life examples of implementing a compliance program successfully.
NAFTA: Understanding the Rules of Origin and Certificate of Origin Requirements
Douglas Cohen
60 Min
Product Id: 703168
This training on trade compliance will help the attendees understand the rules to qualify your imports/exports between United States, Mexico, and Canada. You will also learn best practices on how to complete the NAFTA certificate of origin to avoid penalties.
Insult to Injury During A Crisis: SIM Swap and Other COVD-19 Scams Affecting Patients and Providers
Coy Murchison
60 Min
Product Id: 706491
The challenge for HIPAA privacy and security, cyber security and information security professionals is not alleviated with the OCR’s relaxed standards, during COVID-19. Hackers are using the COVID-19 crisis to steal information, at an alarming rate. Providers are now serving their patients at home, which have weakened security measures in place. Patients and providers information is now at risk as hackers target through telehealth portals.
When Training is a Root Cause: Handling Investigations of Suspected Performance Issues
Mike Kent
60 Min
Product Id: 706351
This webinar will discuss handling situations where training has been identified as a root cause during an investigation. Rather than prescribing the all too common, and largely ineffective, re-training event, discover quick and powerful ways to get at what influenced the individual, and how to address these underlying factors to more effectively prevent recurrence.
COVID-19: Risk Management for HR in a Pandemic
Rebecca Staton Reinstein
90 Min
Product Id: 706511
COVID-19 is not your typical Human Resources Force Majeure! Human Resources Managers are faced with unique risks related to local, State, and Federal, and international regulations and requirements. HR cannot afford to fail to analyze and plan to mitigate risks systematically. Even more problematic is dealing with unexpected risks such as the coronavirus. Learn to create mitigation plans for anticipated risks and a plan to deal with the unexpected. Use some simple tools to analyze risks and prioritize the need for planning. Be confident as you avoid unnecessary "firefighting" and manage risk strategically.
FDA and MHRA Guidance during the COVID-19 Emergency: Medical Devices and Diagnostic Tests
Mark Powell
60 Min
Product Id: 706478
This webinar pulls together current US FDA and UK MHRA guidance covering medical devices and diagnostic tests during the current COVID-19 emergency. Particular emphasis will be given to ventilators and other respiratory aids within the medical device topic.
FDA Inspection Readiness
Susanne Manz
90 Min
Product Id: 706450
Although an effective Quality System should always be inspection ready, many medical device companies make basic mistakes during inspections leading to 483s and even warning letters. This webinar will help you create an inspection readiness plan so you are well prepared for an FDA inspection. This webinar can help you manage inspections efficiently and effectively. You’ll learn about the FDA’s inspectional approach, focus areas, and what documents they will be asking for. A professional, polished, responsive approach sets a good tone for an inspection. You will learn how to present information about your quality system in the most competent and professional manner.
Leading and Managing in Virtual Environments and Home Offices
Axel Meierhoefer
60 Min
Product Id: 706483
Virtual work exponentially increased in the current health crisis as well as constantly grew in the last few years as more and more organizations have people working from virtual and remote locations. They need leadership, management and communication just as it was needed conventionally when we all went to an office environment together. You need to learn how to lead, manage and create connection with your team members and clients. In this new virtual environment, you need to differentiate yourself from all the newcomers and novices that have been forced to try it without much training or experience. We will review the top 7 steps you need to take to become a great virtual manager and leader.
Risk Management - A Process Flow Approach to Converting a Guidance into an SOP
David Husman
60 Min
Product Id: 706414
Attend this webinar to learn how to translate a new guidance or regulation into a working process, and how to use process flow, techniques and templates to develop procedures on your own. The webinar will provide you with a working SOP for Risk Management.
Scheduling and Conduct of Good Pharmacovigilance Practice Audits
Miranda Dollen
90 Min
Product Id: 706387
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.
FDA and MHRA Guidance during the COVID-19 Emergency: Conduct of Clinical Trials
Mark Powell
60 Min
Product Id: 706477
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.
The Use of Statistical Process Control (SPC) Using Control Charts to Maintain Compliance in the Laboratory
John Fetzer
60 Min
Product Id: 706183
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.
Acute Care Case Management: Returning Your Department to "the New Normal" after COVID-19
Bev Cunningham
60 Min
Product Id: 706484
COVID-19 has been a fast-growing, communicable and deadly disease that became a world-wide pandemic. With this disease attacking the US population it changed our lives, and even more specifically, hospital operations. As hospital operations changed, our hospital case management roles and processes changed, as well. As this deadly virus seems to be leveling off, there will be a time that we return to normal. However, our "old" normal will probably not be our "new" normal.
Unsafe Behavior as a General Duty Clause Violation
Michael Aust
60 Min
Product Id: 706449
Have you considered the significant negative impact that unsafe behavior can cause in your organization? The impact goes well beyond the pain and suffering of the injured employee, the workers’ compensation cost and the impact of organizational reputation. Could an unsafe behavior act be an OSHA Act violation under the General Duty Clause?
Wage and Hour Topics: Making Sense of Requirements Affecting Exempt and Non-Exempt Employees
Margie Pacheco Faulk
90 Min
Product Id: 706424
DOL has implemented the Overtime Regulations effective January 1, 2020. Attend this webinar to learn how the new rules impact employers. It will also identify resources and tools that can be used to reduce risk and focus on growing businesses.
Leadership Agility - Why You Need to be an Agile Leader in Today's World
Madonna Swanson
60 Min
Product Id: 706394
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.
Total Product Life Cycle Development (TPLCD)
James W Monroe
60 Min
Product Id: 706460
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.
Artificial Intelligence and HR: AI as a Partner and not a Threat
Greg Chartier
90 Min
Product Id: 706428
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.
VIRUSES IN FOOD: Risk Management Practices (Comprehensive Overview)
Ben Marandi
90 Min
Product Id: 706474
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.