Compliance Training Webinars for Regulated Industries

In this webinar attendees will learn the best practices to attract top Talent from the experience of an active professional recruiter with 37 years of experience with successful experience recruiting from Ivy League Universities to State Universities and Private Colleges.

In this hospital case management webinar attendees will learn the purpose and elements of bundled payments and the role of case managers in the bundle payments system. Also attendees will learn the different metrics and challenges related to bundled payments.

This webinar will cover in great detail how to develop a comprehensive Sexual Harassment Avoidance Policy and effectively train your employees on how to prevent this from occurring in the workplace. The webinar will also deal with how to properly and effectively handle and investigate a sexual harassment claim. Site specific questions and answers along with case scenarios will be given.

This webinar on dose audit test failure for medical device will discuss the various items that should be investigated to determine the root cause, what are the immediate actions that are required and steps to be taken to evaluate product in the field.

This risk based clinical trial webinar will explain the importance of using risk management techniques in clinical research to comply with the latest focus on GCP inspection. It will show you how risk management can improve the quality of your clinical trials and demonstrate the importance of using risk analysis and risk management techniques in clinical trials.

This FDA compliance webinar will help the attendees develop an effective training program and training plans for an organization. Attendees will learn GxP training requirements in US and EU.

In this webinar attendees will learn the critical hard and soft skills required for internal auditors with real-world examples and challenges facing in today's internal audit management. Also attendees will get knowledge on requirements of the internal professional practices framework for internal audit.

In this webinar attendees will learn which products qualify for submissions under 505(b)(2), data that may be referenced, content requirements, and regulatory benefits.

In this webinar attendees will learn how to deal with the challenges and pitfalls that may occur when translating assays as demonstrated in the scientific literature or through internal discovery efforts. While academic research needs only to be novel, interesting and scientifically sound to be published, there may be gaps in the known information about the assay to allow it to go into production use, either for internal industrial research laboratory efforts, clinical trial usage or even for use as a diagnostic assay. This assay will help you learn what needs to be done to shepherd any given assay from the academic world to the industrial world.

Attend this webinar to learn CBP regulations and laws. You will learn how to prepare for, or avoid, possible audit, investigation or further CBP inquiries. An examination of new CBP enforcement efforts that are geared toward changes companies of made to avoid or circumvent the application of 301 duties to their imported products.

In this webinar attendees will learn about FDA’s regulatory expectations for classifying, assessing the risk, testing, and validating a computer system used in FDA-regulated work. Also attendees will learn in detail about the System Development Life Cycle (SDLC) methodology used to approach Computer System Validation (CSV), including all of the phases, sequencing of events, deliverables, and documentation requirements.

Join Elaine Eisenbeisz for a 2-hour webinar as she presents some history behind the many ways of dealing with missing data. She will provide some statistical reasoning on the why and when of applying various techniques in working with missing-ness in data. Elaine will also discuss and demonstrate multiple imputation techniques using SPSS software.

In this HR workforce planning webinar you will learn the latest techniques and case studies which can maximize your human resource and make the organization very effective. The techniques include Strategic Workforce Plans, Design Structures in organizations, Productivity Management, Artificial Intelligence systems and Business Process Re-Engineering.

This webinar training program will discuss how to develop an accident investigation plan, manage cost, and develop realistic schedule. Participants will learn about the interview process, protecting site of incident, determining root cause, and avoidance plan.

This 60-minute session on master verification and validation planning will discuss the major cGMP deficiencies and "must have" elements from the U.S. FDA cGMP, ICH Q9 and ISO 14971 for hazard analysis and product risk management, and show how you can integrate these into a company's quality management system.

The experience mod is the single most important factor when determining workers’ compensation premium. This training program will help employers understand how the experience mod works and how to utilize that knowledge to control your workers’ compensation costs.

This training program will focus on how cell cultures are used for in vitro assays. It will include examples of cell based assay systems and list the advantages of cell based assays. The webinar will help attendees understand the uses of in vitro testing with eukaryotic cell based systems, the parameters to be considered in the development and optimization of a cell based assay and the validation of a cell based assay.

This recruitment best practices webinar will discuss the best way of writing job description to attract the best qualified candidates, the best and creative source of qualified candidates, how corporate marketing can help improve recruitment. It will also highlight other forms of interview questions in addition to the behavioral questions, what should be the best interviewer behavior, how important are reference checks.

This webinar will define human factors engineering and its role in the success of new product development. The session will use real world examples to demonstrate how human factors engineering makes a significant.

This webinar will explain how to apply the theory of lean documents and its corollary theory of lean configuration to present a fresh approach to controlled document system for a life sciences manufacturing plant.