Compliance Training Webinars for Regulated Industries

This webinar will give insights on regulations and CMS interpretive guidelines which are now part of the hospital CoPs on telemedicine credentialing. It will discuss CMS mechanism for all hospitals to use proxy credentialing with Medicare-certified hospitals or other telemedicine entities. It will further discuss why written agreement is required, and insights on the requirements in the written agreement. It will also provide insights on standards, Joint Commission has on telemedicine in the leadership chapter.

This HTSUS & schedule B code webinar will discuss on how to use Section and Chapter notes. Attendees will also become familiar with the scary General Rules of Interpretation, all of which will become non-threatening and very useful to you. Attendees will learn the basics of import (and export) product classification. Lastly, attendees will learn how to approach CBP for help with classification determinations.

This webinar is designed to help banks and credit unions get smart about opening online accounts (Covers both new consumer and business accounts) . It will evaluate practical risk management strategies institutions can use to build a program appropriate for their risk appetite, validation and verification strategies, due diligence. How to support online account development with the appropriate products, social marketing campaigns, and effective risk strategies.

This webinar will cover the system suitability requirements and recommended adjustments to specific chromatographic systems in the USP monographs based on General Chapter <621> Chromatography. We will also discuss the most recent updates on proposed harmonization of this general chapter with EP and JP and how to implement the procedures after the change is effective.

In this webinar our expert Dr. Mike Colvin will discuss how to use ISO 14708-3 standard which is applicable to active implantable medical devices intended for electrical stimulation of the central or peripheral nervous system and contains particular requirements to ensure basic assurance of safety for both patients and users.

This webinar will cover effective and efficient ways to transition from paper to electronic records in a regulated environment. It will address compliance issues, complexity in decision making and implications specific to the pharmaceutical industry.

In this webinar attendees will learn the common problems associated with coding applications, their implementations and their monitoring in clinical practice.

In this session, international trade attorney Martin Behr III will teach you how to avoid AD and CVD problems. This session will help you gain critical knowledge about AD and CV so that you may exercise reasonable care while importing products into the United States and thus avoid costly and aggravating problems with U.S. Customs and Border Protection, the U.S. Commerce Department, and other governmental entities.

This training on credit card surcharges compliance will discuss how the recent changes in law will affect end-user organizations. It will also provide attendees with the tools necessary to review and deal with any potential surcharge/checkout fee situations.

This training will help you understand FDA expectations for reduced testing of Pharmaceutical & Medical Device components and will develop your confidence in maintaining control of supplier quality.

This regulatory reporting webinar will discuss the importance and characteristics of a regulatory reporting system. It will also explain how to create processes to work seamlessly with it along with the planning and designing the system to meet the requirements of complaint and adverse event reporting accurately and timely.

This Webinar will discuss how to create a plan for correction of survey deficiencies which includes the incorporation of the agencies Quality Assurance Performance Improvement indicators to ensure ongoing compliance. A focus will be on plan of corrections for the new Conditions of Participation that were implemented on January 13, 2018.

This 90-minute webinar on laboratory investigations will explore successful approaches to laboratory investigations of out of trend results and also explore approaches which may have potential for pitfalls.

This Sunshine Act reporting webinar will discuss new requirements for manufacturers of healthcare products related to report of certain payments and items of value given to physicians and teaching hospitals. It will discuss the reporting format, exemptions and timeline for compliance and practical solutions to most common situations prevalent between sponsors and investigators.

This contractor safety webinar will teach how to create an effective contract safety program which includes OSHA requirements and steps like contractor prequalification, Contractor Safety Orientation and other site-Specific Questions and Scenarios showcasing best practices to follow for a comprehensive contractor safety program.

This 90-minute webinar on Disinfectant Qualification Studies will teach you disinfectant testing methodologies, provide examples of disinfectant efficacy tests and show how to troubleshoot problems related to disinfectant efficacy testing.

This CBP webinar will discuss the general compliance requirements, the likelihood of a CBP inquiry and how to identify potential vulnerability by conducting internal review, testing your compliance and most importantly what to do when targeted by CBP.

This webinar will review the CTD format requirements including documentation and technical requirements for an eCTD submissions. It will help attendees prepare for implementing the FDA upcoming mandates on e-submissions.

This webinar will discuss the fundamentals of current base pay plan, market pricing, compa-ratio, grades, and ranges to give your organization the means to confidently build a competitive and effective pay structure.

This Statistical process control webinar will discuss the 10 elements which will enable any company to improve their SPC and realize the benefit. It will discuss how to identify and use right systems, charts, controls limits, sampling and what process improvements required to achieve more from your SPC program.