Compliance Training Webinars for Regulated Industries

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.

This webinar will help you understand the significant differences between qualification and validation of an analytical method, the expectations and requirements of each, and their place in the analytical method lifecycle.

This 90-minute webinar will help you understand the application and requirements of OSHA Hazardous Energy Control (29 CFR 1910.147, 29CFR1910.333), commonly known as Lockout / Tagout (LOTO), and the topics that have been interpreted and reviewed in the compliance guidelines.

This FDA validation training will describe methods for planning and executing spreadsheet validations that satisfy FDA requirements.

This webinar will provide a detailed information on the critical requirements of ISO 17025 and recommendations for cost effective implementation. You will learn steps towards laboratory accreditation and how to prepare for an ISO 17025 audit.

This 90-minute webinar will help you understand the competence and training requirements in the Quality Management Systems for medical devices, especially FDA QSR, ISO 13485, and even ISO 9001.

This webinar will build upon a basic knowledge of noise monitoring and hearing loss to help in understanding the instruments used in performing noise monitoring and how best to use them in developing and implementing a practical strategy for performing noise monitoring.

This webinar will review the principal differences in regulations governing investigational device (IDE) studies and drug (IND) studies and help you understand where the regulations diverge and how this impacts the design and execution of device studies.