Compliance Training Webinars for Regulated Industries

This training on assessing risk management processes will explain the IPPF Internal Audit Standard 2120 in detail, highlight recent updates to the standard, discuss how to comply with it and use it to assess the effectiveness of risk management processes at your organization.

This ISO 13485 requirements training will provide guidance to medical device companies in developing an adequate Quality Management System (QMS) in accordance with ISO 13485 and FDA expectations. This webinar will also benefit medical device companies that are planning to market their products in Europe.

This webinar will address the statistical basis for sampling and testing. Topics will include two and three class sampling plans, as well as the operating characteristics of individual plans with primary focus on interpretation of results, based on the limitations of sampling plans and microbiological methods.

This IT Audit webinar will demonstrate how to evaluate your Technology Investments’ implementation “readiness” thereby reducing your risks during implementation along with the general audit steps, Audit risk assessment, Audit objectives, Audit approach, Audit testing, Audit report etc. It will also cover IT Investment Management issues and how to improve the organization’s IT results.

This webinar will provide an introduction to FDA’s regulation of product labeling and promotion; and the Agency’s position with regards to off-label promotion and how the Court’s decision in the Caronia case might affect the off-label promotion of Rx drug products and medical devices.

This HIPAA risk analysis webinar will discuss how to do HIPAA security risk analysis, the various security policy consideration for laptops and portable devices, and their security. How to use risk analysis tools and techniques to create, document and manage policies. HIPAA Audit Protocol will be presented, and its use as a compliance tool will be explained.

This webinar will cover how companies can deter the likelihood of AR frauds through strengthening internal controls by numerous methods to detect, prevent, and deter frauds. We’ll focus on the most common accounts receivable schemes and the top ten internal controls that prevent fraud.

This training on preserving meat will explore the techniques and methods of smoking and curing meats commercially and its benefits, health risks and HACCP requirements. It will also cover packaging, storage and shipping considerations for mass produced cured meats.

This social media compliance training for healthcare companies will cover the legal and regulatory requirements governing the use of social media. A scenario-based learning approach will be used to show how to create a successful social media team by selecting members from relevant stakeholders, and prepare social medial policies and procedures.

This webinar highlights the evolution of Enterprise Risk Management (ERM), the importance of ERM in meeting board fiduciary responsibilities, and the rationale and mechanisms for ensuring effective risk management through the board.

This webinar for food processing will cover the overview of systems necessary to reduce the risk of foreign material contamination, associated guidelines, HACCP and prerequisite programs followed by investigative techniques and a customer and team response plan.

This webinar will highlight the evidence normally requested during audits and inspections of biotechnology analytical labs. You will learn how your laboratory's biotechnology analytical methods can fulfill stated or implied regulatory requirements (the US FDA refers to these as the “C” in CGMPs).

This HIPAA HITECH webinar will help you understand the requirements of HIPAA internet technology security (specifically to the electronic storage, transfer and use of patient information) and discuss the preparation for the Health Information Exchange (HIE) Network. Instruction as to best practices procedurally and electronically, to maintain a secure environment.

This BYOD and information security webinar will help you explore the current state of BYOD in the workplace, the need to evaluate the risk to the organization prior to deployment, the critical need for identifying and communicate a strong legal strategy, select the right mobile device management solutions (based on risk assessment), ability to develop and implement strong BYOD policies, is BYOD right for your organization, and how the “Cloud” impacts information security with BYOD.

This webinar will discuss the various safety metrics used to measure safety performance, what they really measure, and why tracking metrics often does not deliver the improvements in performance desired.

This 90-minute training will discuss recent OFCCP enforcement trends and regulatory initiatives and review these against your current practices and procedures to ensure your company is audit ready. It will also cover the proactive steps that federal contractors can take to prepare for the impending rules.

This comprehensive training package of 6 courses is aimed at helping pharma/drug companies to be compliant and streamline the supply chain planning, processes, risk management etc by maintaining regulatory guidelines.

This webinar on business continuity planning for healthcare organizations will discuss the major drawbacks to business continuity planning projects as they are currently done, and describe a simpler, more efficient approach to getting them done and implemented.

This medical device process validation training will use recent warning letters to explain the regulatory requirements for process validation and what FDA Investigators look for. It will cover process validation components (IQ, OQ, and PQ), and the content of protocols and reports.

This training on C-TPAT will explain why and what you need to do to participate in the C-TPAT (Customs-Trade Partnership Against Terrorism) program. It will cover all aspects of the C-TPAT program and help existing members to prepare for validation or revalidation.