Compliance Training Webinars for Regulated Industries

This webinar will equip attendees with the knowledge necessary to efficiently design and enhance GRC activities across the organization based on established GRC standards.

This webinar will provide you practical tips on handling the OSHA inspection process with an inspector. You will learn about the types of inspection, the tools you can use, what information to discuss with an OSHA inspector, what records to show and about your rights and responsibilities.

This 90-minute webinar will highlight actual examples of travel fraud that happen in organizations and focus on internal controls that you can have in place to prevent fraud related to travel and subsistence claims.

This 90-minute webinar will explain how HIPAA audits are conducted, what the auditors will look for, what they will ask and how. This training will prepare all HIPAA covered entities and business associates to be fully in compliance and be prepared for an audit at any time and to quickly respond to audits.

This 120-minute webinar will help medical device manufacturers to understand what you need to do to ensure that your process, the methods, and the procedures that you have established to implement the requirements for design controls are in perfect order.

This webinar will provide processes and procedures to all medical device companies that are thinking of transferring equipment, molds, dies, systems and processes to contract manufacturers. It will follow a recent successful case study in the medical industry.

This webinar, by a former USFDA executive, will provide an insider’s insight into the US FDA's pre-approval inspection program, its objectives and the roles and responsibilities of the entities involved in the program.

This 90-minute webinar will summarize current and emerging cyber-threats and provide latest insights and advice from experts on how to protect your organization from individuals - both inside and outside of your organization.

This 90-minute webinar will outline the common deficiencies in relation to method validation, for pharmaceutical products, outline regulatory requirements and the change control process needed to stay in compliance.

This webinar will provide you with a step-by-step guidance on how to deal with complex situations in the workplace that involve conflicts between religious beliefs and work obligations.

This webinar provides a behind-the-scenes look at how trial lawyers think and operate. It will provide you the understanding necessary to take steps to counter the tactics of trial lawyers and also keep your businesses off the trial lawyers’ radar.

This webinar will define and describe the principles of leadership. It will provide examples of leadership styles that will allow the participants to determine their own leadership style as well as the styles of their managers, peers, and subordinates. We’ll discuss how situational leadership can be an effective leadership style.

This webinar will outline the best ways to identify your trial needs to select a CRO, the right people to talk to, contract negotiations, ownership and accountability and challenges in the Sponsor-CRO relationship.

This webinar will review the first steps of creating a food safety and HACCP program in an on-going operating business. You will understand the key areas to address when setting up or modifying HACCP or food safety programs, with minimal staff.

This 5-hr virtual seminar will provide a step-by-step procedure for conducting an efficient, effective, and credible internal sexual harassment investigation.

This webinar will guide you in establishing the right safety metrics for your organization. You will learn about steps you can implement to improve your organization's safety performance.

This webinar will cover definitions, responsibilities, regulatory requirements and strategies to conduct Investigator Initiated (Sponsored) Trials - ISSs. It outlines the processes a company or investigator must undertake to be able to conduct such a clinical research study in humans.

This 120-minute webinar will cover best practices and standardized processes, outlined in ISO 14971, for managing risk in medical devices. You will learn from the shared experience and examples provided by the speakers on how to implement proper and effective risk management processes and practices at your company.

This 90-minute webinar will clarify your confusion about Test Article Characterization for GLP drug studies. You will learn the correct way to use GMP characterization data in a GLP study, understand how to characterize a medical device as a test article, learn the common mistakes made in test article characterization and the basic requirements for drug and device stability testing.

This webinar will help you to develop and implement a cost-effective, yet practical strategy, for Industrial Hygiene (IH) monitoring consistent with prevailing standards of practice. You will learn how to select the appropriate sampling and analytical methods for your IH monitoring plan.