Compliance Training Webinars for Regulated Industries

Health care organizations should be monitoring and auditing their existing call coverage arrangements to ensure they are compliant with regulatory requirements in case they are challenged. This training session will provide an overview of the Anti-Kickback and Stark Law, including 2016 changes and updates.

In this training program, the instructor will discuss case studies on the types of forklift safety mistakes that are found in the workplace. He will also provide strategies on how to actively engage your workforce to improve the safety culture of your workforce.

This GMP inspections webinar will review what to expect during the agency inspection and how to successfully and efficiently streamline and manage the inspection, including adequate follow-up during and after the inspection.

This webinar will help you gain a greater understanding of regulatory and compliance requirements and how the early product lifecycle requirements establish the basic groundwork as a foundation from product development to commercialization continuing to out commercialization and product discontinuation.

This training program will explore how using service level agreements along with key performance properly will enable a shipper to drive continuous improvement in their supply chain. SLAs and KPIs will also ensure that agreed to, objective measurements are being used to judge 3PL performance. An SLA along with the proper KPIs will allow shippers to create incentives, disincentives and exit clauses based on performance.

In this webinar, attendees will learn how lyophilization cycles are developed, how lyophilizers work and how they are controlled and what is important to FDA and other regulatory bodies in the inspection of lyophilizers and in the validation process.

This webinar will discuss the strategy to conduct safety trainings and provide practical methods and techniques to make safety trainings more effective, educational and entertaining. Instructor will explain how to make trainings interactive, engaging and deliver required results and how to measure effectiveness.

This training program will guide attendees in writing effective Standard Operating Procedures and Work Instructions. It will also discuss how to assess and write to the audience and how to review and revise SOPs and Work Instructions.

The training program will provide insight into complying with the key QMS requirements for organizations selling medical devices in Canada.

This clinical research training will explain the Institutional Review Board (IRB) models. It will discuss the regulatory framework for IRB review including 21 CFR 50, 56 and 45 CFR 46.

This training program will explain how we ascertain the difference between circumstances in which a service provider is an employee (and a principal is an employer) and circumstances in which the service provider is an independent contractor (and the principal is a client).

This training program will identify regulations and guidelines pertaining to data management in clinical research. Attendees will learn to translate the regulations and guidelines into practical application for each stage of the clinical trial: start-up, ongoing study management, and study closure. The program will also discuss the do’s/don’t for data management activities through real-life examples.

This webinar will help you identify required, minimum safety training requirements under OSHA and 29 CFR 1910 for General Industry organizations. Participants will understand trainer requirements for providing instruction on safety topics. The Instructor will discuss the frequency of training topics required and will explain the training matrix.

This training program will explain what the critical areas and elements of vendor oversight are and how you can set such a system up for yourself at your company.

This training program will take an in-depth look at various clinical research contracts designed for different purposes. Understanding each type including what is being protected and who is being protected is an important part of ensuring compliant administration and management of clinical research activities. Beyond the legal terms, this course will examine the standards for accredited organizations and best practices for ensuring the broadest protections for study participants.

This training program will offer a comparison of RCRA and California hazardous waste characterization. It will detail the enactment of the California Hazardous Waste Control Law in 1972 before RCRA in 1976. The course will also discuss permits required to treat most hazardous wastes that would be exempt from permitting under RCRA.

This compliance training program will focus on key elements of the Americans with Disabilities Act (ADA). It will provide insights on amendments to the act and provide instructions on writing ADA compliant job descriptions.

This training program will help attendees prepare to work within Food Safety Modernization Act guidelines and understand how they will be impacted, and how to adapt. The program will also offer best practices to make your supply chains meet the rising demands of consumers.

This training program will help attendees identify why silos exist and understand how to eliminate them. It will also examine why hospitals have lost focus on the patient and the importance of strategic direction and strategy deployment.

This training program offers an objective, thorough review of the basics of state regulation of a given profession, with an emphasis on the individual health care practitioner. Among other topics, the webinar will discuss sources of legal requirements for professional licensure; difference between government licensure and private certification; and detail state licensure mandates as applied to individual health care practitioners.