Compliance Training Webinars for Regulated Industries

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.

This webinar will be a detailed look at regulations which are in place on Nov. 28, 2017. The new survey process using the new requirements could take place in your nursing home anytime and will be evaluating both Phase 1 and Phase 2 requirements. Be sure you understand the Phase 2 regulations and know where your home stands in complying with them.

This webinar, by an ex-FDA, will cover Good Data Integrity Practice for GxP environments. Participants will understand what FDA looks for with regard to data integrity, what may need to be audited, the new guidance and application of data integrity, and relevant regulations for data integrity

This webinar will unravel the Center for Medicare and Medicaid’s (CMS) guidelines on billing for “incident to” and Split/Shared services and will discuss the many benefits of doing so, while cautioning practices about compliance risks. The audience will be helped to understand the requirements when billing these types of services and to understand the documentation and supervision requirements of the physician.

This webinar will discuss the key things required by U.S. Customs & Border Protection (CBP) when they conduct a focused assessment (import audit), how to identify potential risk factors related to import compliance which can subject you to severe penalties and delay in clearing goods through CBP. It will also provide recommendations for some best practices that may resolve non-compliant import procedures and documentation or improve existing procedures.

This webinar will help you master pivot tables in Excel 2007, 2010, 2013, and 2016. Learn tricks and traps of working with pivot tables to help ensure accuracy of reports and convert obsolete Excel spreadsheet files to modern workbook formats.

This webinar will discuss how to counsel mothers about adverse effects of taking medication while breastfeeding. How to identify CBS drugs that are usually safe to use while breastfeeding.

This webinar will discuss the steps to execute internal GMP Audit, how to get all departments for acceptance and how to communicate audit findings specifically when it is serious and quality needs confirmation of acceptance and resolution.