Compliance Training Webinars for Regulated Industries

This Project Management training for Auditors will help you understand how to apply project management principles to auditing to ensure efficient and effective quality assurance of drug development.

This webinar on supplier controls will provide you the information you need to assure your supplier management program is in compliance with the latest FDA, European and international guidelines requiring a risk-based supplier management program. We will look at how to improve your supplier management system to meet both the FDA and ISO expectation while potentially reducing your cost of compliance.

This webinar will help you to build, implement, and maintain strong credit culture. This course offers 14 tools to test and check the strength of the organization’s credit risk management and techniques for remediating and improving credit culture and credit risk management.

Attend this webinar to learn payroll best practices (handling of state taxes, wage and hour law, and garnishments) when an employee lives in one state and works in another, or works in two or more states simultaneously. This Includes determining liability as an employer, reciprocal agreements, resident and nonresident taxation, Form W-4 equivalents, state unemployment insurance, wage and hour law requirements and garnishment withholding.

This training program will examine the approval process for drugs, biologics and devices and elaborate FDA submission requirements and guidances. It will also discuss electronic regulatory submission and gateway for FDA and FDA eCTD guidance and specifications.

This webinar focuses on the verification and validation planning and execution of software, after basic developmental testing and de-bug. It includes COTS (commercial off-the-shelf) and the growing field of "cloud"-based software. A suggested FDA model (mandated for submissions) will be evaluated, implemented, with V&V documentation and test case examples. Also attendees will learn the most recent issues the FDA has had in this area, and remediation approaches.

Attend this webinar to learn about compensating controls with specific examples and what are the segregation of duties controls. You will also learn how to implement compensating controls to reduce risk and prevent fraud in your internal controls programs.

Attend this webinar to learn the role of the cyber communication plan during a cybersecurity incident. You will learn the type and elements of a cybersecurity communications plan and how to reduce the costs associated with communications during a cybersecurity incident.

This webinar will help you in creating Social Media strategy for your business at all level of management. You will learn Social Media Guidelines, Social Media Do’s and Don’ts, Social Media Policy, Reputation Management and how to avoid Social Media Mishaps.

This Microsoft excel training program will help attendees to understand the financial modeling concepts to model their capital expenditure projects and the methods for CAPEX analyses. Attendees will learn how to prepare and present outstanding, professional-level CAPEX models using special Excel tools.

This healthcare documentation webinar will discuss how to create a lawsuit-proof, auditable nursing documentation and how to maintain compliance over the course of the document life-time. You will learn how to de-risk your documentation so as to withstand legal scrutiny.

This 90-minute webinar will help you gain an understanding of the regulatory background and provide complete guidance starting from the planning and writing requirement specifications to vendor evaluation, installation and operational qualification and continued testing while in routine use. The webinar also covers the instrument qualification and system validation processes.

In this webinar attendees will learn the GLP requirements for records archiving, discuss common errors many companies make when archiving GLP record, the options for archiving electronic and manual records, and how archiving practices may impact an audit. Also attendees will receive tips on proactive steps they can take to avoid common pit falls and how records readiness can facilitate a smooth audit process.

This webinar will explain how to select an effective Chief Compliance Officer (CCO) or Chief Risk Officer (CRO) best suited to the position. It will also review the skills needed to communicate the essence and structure behind a good compliance program.

This CMS QAPI standards webinar is designed to help surveyors assess compliance with the hospital CoPs for QAPI(Quality Assessment and Performance Improvement). This worksheet is used by State and Federal surveyors on all survey activity in hospitals when assessing compliance with the QAPI standards including validation and certification surveys.

This webinar will discuss various container closure systems that are available for use with liquids and lyophilized products, the components that constitute a container closure system and also cover specialized delivery systems.

In this HR compliance webinar attendees will learn the behaviors, consequences and myths about workplace bullying & how to develop an effective strategies for dealing with workplace bullying and steps to eliminate workplace bullying for building a healthy workplace where employees can thrive.

This training program will provide guidance in recognizing, investigating and reporting suspicious activities. It will also discuss instructions on implementing and maintaining an enterprise wide compliance program to safeguard the financial system from illicit use and combat money laundering and promote national security through the collection, analysis, and dissemination of financial intelligence to the regulatory authorities.

In this Risk Management webinar attendees will learn the risk management guidance on third-party relationships provided by the OCC Bulletin 2013-29 and how the banks continue to increase the number and complexity of relationships with both foreign and domestic third parties such as outsourcing entire bank functions, outsourcing lines of business or products, single third party to perform multiple activities, address deficiencies and engage directly with customers.

This training program will explain the rationale, the legal requirements and some methods commonly used for reprocessing and validating reusable medical devices.