Compliance Training Webinars for Regulated Industries

This training will help you understand the concept of workplace bullying. You will understand the similarities and differences between illegal harassment with legal workplace bullying & how to handle them. Attendees will learn tools for managing bullying at work.

This Enterprise Risk Management (ERM) training will help attendees learn an innovative approach for integrating ERM risk assessment, crisis management, and business continuity. Attendees will leverage this approach to think strategically about potential risk identification blind spots and simultaneously evaluate day-to-day operating assumptions that can preserve value and enhance process maturity.

This training on healthcare compliance will teach the attendees best practices for conducting a self audit of excluded providers. Learn how to prepare and conduct an audit to ensure compliance with this important mandate of Medicare participation.

This webinar will provide a comprehensive overview of FDA regulations for cosmetic products. It will help you understand how to be compliant in manufacturing, labeling and advertising of cosmetic products, and thereby ensure successful FDA and state inspections.

This GLP compliant assay training will help attendees deal with the challenges and pitfalls that may occur when translating assays as demonstrated in the scientific literature or through internal discovery efforts.

This webinar will cover how to have an effective Annual Risk Assessment (ARA) and internal audit’s role in ARA. You will be able to identify the appropriate risk framework, their risk rankings, and balancing their available resources.

In this Foreign Corrupt Practices Act (FCPA) webinar training understand the prohibited and exempted actions as per FCPA act, how to find the non compliance issues and how to implement FCPA compliance policies and procedures in your organization.

This Basel III training will focus on the key aspects of Basel III and highlight how it differs from those in Basel II. It will discuss additional compliance requirements for Basel III, the costs involved, implementation timelines and provide a framework for end-to-end implementation.

This 3-hour training will review and compare FDA’s Establishment Registration and Product Listing Requirements; and available User Fees, Fee Waivers and Marketing Exclusivity for Drugs, Biologics, Medical Devices, Food, Tobacco and Animal Health Products.

This webinar will show you how to audit your GRC program (governance, risk and compliance) and how to evaluate its design and operating effectiveness.

This webinar will provide an in-depth understanding of California specific laws, affecting food and other product manufacturers and marketers, such as the Prop 65, the Green Chemistry Initiative, and the Rigid Plastic Packaging Act. We will discuss these laws, how to comply with them and avoid litigation.

This HR compliance training will provide attendees simple but powerful tools for creating and implementing an effective human capital strategy and plan which will drive out costs, increase Return on Investment (ROI) and get the results one requires.

This webinar on drug price reporting will discuss the changes to the Medicaid Drug Program and its impact on pharmaceutical and biotech companies.

This 3 hour virtual seminar will help you create an integrated medical device software development process that will meet IEC 62304 and ISO 13485 design control requirements, and generate the documentation needed for software as part of a FDA submission.

This webinar will cover regulatory requirements for archiving clinical trial documents, both paper and electronic records. It will focus on the key components of a digital preservation strategy to ensure the ongoing retrievability and accessibility of clinical trial electronic records.

This training on marketing of beverages, fruit juice and sports drinks will focus on FDA’s labeling regulations and requirements, FTC enforcement of advertising claims, and recent developments in consumer class action lawsuits involving beverages. Attendee will learn best practices to ensure compliance with FDA and FTC regulations.

This webinar will review recent inspection focus areas by Cal-OSHA inspectors, discuss how you should prepare for the inspection, and demonstrate proven strategies that will help you be successful both during the inspection as well as afterwards if there are violations and citations to deal with.

This GRC training will provide the attendees best practices for auditing their compliance team. Learn how to identify the strengths and weaknesses of your internal compliance departments.

The webinar will familiarize participants with the FDA's Refuse to Accept Policy for medical device 510(k)’s and help you ensure that your 510(k) application is not rejected for lack of administrative completeness.

The webinar will discuss best QC practices and procedures for verifying the suitability and performance characteristics of microbiological media and reagents.