Compliance Training Webinars for Regulated Industries

This food allergen training will provide the attendees with insights into the sources and control of common food allergens in the food processing operations.

This webinar will offer risk management professionals practical methods to translate their risk-language or risk-speak into simple language that business operators across the organization can understand and comply with.

This virtual seminar will start by evaluating important areas for regulated companies to focus in 2013-2014, based on the U.S. FDA’s recent "Strategic Priorities" initiative. The second-half of the session will discuss how FDA's global initiatives affect supplier chain management and vendor audits and how you can prepare to address them.

This webinar on FDA's food import oversight will focus upon regulatory and enforcement issues surrounding the importation of food products. It will review FDA’s current sampling, inspection detection and seizure programs.

This webinar for medical device manufacturers will discuss the CDRH interpretation of the GHTF guidance and how manufacturers should develop process validation plans and conduct production process validation.

This training on ISO 14971:2007 will help you understand the risk management process for medical devices, including risk analysis, risk evaluation, risk control and post-production information.

This webinar on handling FDA inspectors will discuss practical tips to cope with a difficult FDA compliance officer or inspector. You will learn how to wiggle out of complicated situations, make legal arguments and challenges to the FDA agent and use meeting requests and other tools to ease tensions.

This food contamination control webinar will provide in-depth information on the currently available approaches to the prevention, control and detection of foreign bodies in foods. It will use example scenarios to discuss what to do when a foreign body incident has occurred.

This 3 hour virtual seminar on China regulatory compliance processes for life science products will discuss the regulatory structure and requirements for compliance against China’s CFDA regulations for Pharmaceuticals, Medical Devices, Biologics and Combination Products.

This webinar on social media compliance in a healthcare setting will explain how you can use social media to communicate with patients while ensuring that you meet the privacy, security and compliance aspects of handling sensitive patient data. It will also discuss the documentation needed to explain proper social media adoption, during an OCR audit.

This international trade compliance training will explain each of the areas covered by the 11 Incoterms and how each one works. The course will also explore the risks and advantages of each Incoterm, writing contracts of sale, reviewing purchase orders, proper export sale documentation and more.

This BFSI compliance training will assist participants, including bankers, regulators and board members to better understand and study the requirements for an effective and efficient governance program for a financial institution. It will highlight the issues of governance for banks and financial institutions and the principles and implementation factors to consider.

This webinar will help you understand and comply to the Unique Device Identification (UDI) policies, both current and the upcoming FDA requirements for importers, manufacturers and hospitals.

This HIPAA compliance training will help healthcare business associates understand the risks associated with handling Protected Health Information (PHI) and show how to implement the steps required to mitigate the risks to secure PHI and comply with new HIPAA/HITECH omnibus rule.

This webinar will discuss the practical aspects of a good Respiratory Program and help you understand when and where respirators are to be used, together with the right respirator for the hazard that employees are subject to within your work space.

This webinar explains concepts required for a calibration program that satisfies FDA’s Quality System Regulation (QSR), ISO 13485, and ISO 9001. It defines the concepts of accuracy and precision that define the measuring equipment’s requirements. It also explains the meaning of traceability.

This webinar will cover FDA and FTC requirements for substantiating labeling and advertising claims. It will cover best practices in substantiating your claims, legal developments, and defenses.

This training on OSHA regulations will explain the requirements of the new hazard communication standard and globally harmonized system of chemical classification. It will also provide you tools to implement the updated regulation in your organization’s facilities.

This webinar will highlight the strategies for selecting and effectively managing the customs broker. It will help importers understand the role and importance of good brokers in complying with customs requirements.

This webinar will provide attendees the tools and tips to integrate ethics and compliance risk into an organization’s risk management program. It will explain the role and importance of integrating such ethics and compliance risks into an organization’s overall enterprise risk management framework.