Compliance Training Webinars for Regulated Industries

This webinar will identify components of a valid letter of guarantee for the food processor and the determinations that food packaging supplier must make in issuing the guarantee, certifying that they comply with US FDA regulations.

This 4 hour training will focus on best practices in design reviews and show how you can add high value to your products and processes by improving the performance while reducing the life cycle costs significantly.

This webinar on Hazard Recognition Techniques will help increase your awareness of workplace hazards, provide meaningful and useful hazard identification procedures, methods to perform 'hazard' surveys that reduce risks that can lead to worker exposures to hazardous materials or injuries.

This FDA Pre-Approval Inspection training will focus on the purpose and scope of pre-approval inspections, the consequences from them, and keys to a successful FDA pre-approval inspection.

This webinar on Wellness Programs will show you how to distinguish between real and fabricated wellness reports by identifying phony metrics, and choose a wellness program that best fits your organization.

This full day GCP training course will provide comprehensive learning on the Good Clinical Practices of Research involving human subjects. It will cover all key areas including recruiting study subjects, the Informed Consent process, Adverse Event Reporting and preventing protocol deviations.

This webinar addresses new test methods for quantifying migration of Printing inks on food packaging materials into the packaged food and how they affect food safety law compliance.

This DMFs (Drug Master Files) training will discuss the current review and enforcement climate within FDA and the manner in which drug master files (DMFs) are reviewed by FDA personnel. Besides the US, the use of DMFs in the EU, Japan, Canada and Australia will also be discussed. Similarities and differences to the U.S. system will be highlighted.

This webinar will explain the different types of Personnel Files. Attendees will learn about the types of personnel files that need to be separated from other types, and those that require separate security measures.

This training will outline practical steps to design medical device software that does not compromise on performance reliability and patient safety, thereby preventing product recalls.

This webinar will help you Gain a better understanding of your responsibilities as an exporter under the ITAR. Learn about the laws governing defense articles and services, how to comply with the regulations, and develop an effective ITAR compliance program.

This Food Recall training will help you create a robust process for planning and conducting a food recall and crisis communication. It will help each department anticipate their roles and responsibilities so your company’s response will be effective and swift.

This Health Information Privacy Compliance training will provide an outline and roadmap for developing a risk-based approach to compliance.

This training on UK Bribery Act will help you understand its requirements and how it will impact your organization. Learn how to identify areas of risk, proactively mitigate them to avoid significant fines and loss of reputation.

This training on auditing of software vendors for FDA compliance will explain the types of audit and its use in qualifying and selecting vendors. It will discuss sample forms and checklists which may be used by the participants for observations, recommendations and remediation.

This Clinical trial auditing training will provide valuable assistance how to conduct clinical trials both using internal resources and also those that outsource the function to CRO’s in pharmaceutical and biotech industries. How to assure your clinical trials are in compliance and meet the agencies requirements.

This 4 hour virtual seminar will provide a solid understanding of the USP, its sections and how they are inter-related. Attendees will also learn how to be aware of changes to the USP, and how to influence them.

This Anesthesia Services Compliance training will help you understand what auditors are looking for when they review your anesthesia documentation.

The presentation will consider potential impacts of the rule on regulated and unregulated vendors, and providers. This session will survey the market affected by the proposed rule, and define the common components and capabilities of these systems.

Learn about last changes in Canadian ethics regulations, understand how to apply the change in the day-to-day work.