Compliance Training Webinars for Regulated Industries

This training program will discuss the planning and preparation needed for an independent review, or any other review of an AML/CTF program, and consider the stakeholders who need to be identified and managed throughout the field work, the impact on the business as they continue with business as usual as well as the likely areas where issues may be found. Understanding the process of an independent review provides the opportunity to test the implementation of your program before hand and call out some issues that need focus before any review commences.

The webinar will focus on the path most health care organizations in the country have taken to integrate along with the internal fragmentation that often remains after the deals are over. It will also discuss emerging best practices to manage fragmentation and risk.

This webinar will explain how to create, develop and manage Design History Files (DHFs), Device Master Records (DMRs), and Design History Files (DHFs) using lean document and lean configuration methods.

To be certified with BRC Global Standard; a Food Manufacturing needs to implement Processes that address all the Requirements of the Standard. This Webinar lumps together the Requirement including Records & Documents needed to successfully implement BRC.

This VFD Final rule webinar is to give you better understanding what changes apply to you either as veterinarians, food animal producers or distributors.

This presentation, will aid manufacturers of medical devices who intend to modify a 510(k)-cleared device or a preamendments device subject to 510(k) (i.e., “existing devices”) during the process of deciding whether the modification exceeds the regulatory threshold of 21 CFR 807.81(a)(3) for submission and clearance of a new 510(k).

Learn 10 major difference between Cal/OSHA and Federal OSHA and how to respond to it in case of OSHA inspection.

This webinar will teach you how to design, build and test medical device software in preparation for the successful 510k submissions. It will cover medical device software user requirements, software architecture, design, unit testing and more.

This webinar will examine the rational use of biopharmaceutical principles to design a drug product that will optimize drug delivery to achieve the therapeutic objectives of the drug.

This 90-minute webinar will discuss current trends concerning international construction arbitration Attendees will learn the ins and outs of international construction arbitration including twelve trends current in this forum globally as well as six developing trends that may have the potential of changing today’s international construction arbitration.

This training session will provide the guidelines to formulate effective SLAs for services needed for all support areas (Accounting, Human Resources, Information Technology, Supply Chain, etc.) whether the support is provided internally or external (outside) service providers. Also attendees will learn the importance of “best interest” when SLAs are constructed with external (outside) service providers.

This webinar will help attendees to learn the current issues and changes to BSA/AML compliance obligations and the common regulator findings related to payments and customer risk.

This webinar will discuss the different types of Grinding Wheels and what the OSHA Requirements are to protect Employees from injuries and fatalities.

Attendees that need to perform bioavailability (BA) and bioequivalence (BE) studies for INDs, NDAs or for NDA supplements should attend this training. They will learn the requirements of such studies, per 21 CFR 320 and all other relevant regulatory documents.

This environmental regulation training will explain in details the differences between California Environmental Regulations and U.S. EPA and Other State Requirements.

This webinar will help attendees to understand how an administrator can order an employee to undergo a drug test and what are the steps to reduce the risk to keep an employer’s drug testing program compliant.

This webinar addresses the compliance challenges in data privacy. It will also discuss the key drivers for developing a formal data privacy program and the elements of a data privacy compliance program.

This training program will discuss posting and notice requirements, recordkeeping requirements, anti-retaliation requirements and penalties for failing to comply with the mandatory paid sick leave requirements.

This webinar will cover what Distracted Driving is and how to prevent it in your workplace and fleet. This webinar will cover how to effectively implement a Distracted Driving Prevention Program and discuss best practices to implement effective Distracted Driving prevention techniques.

Attendees will leave the course clearly understanding of all the requirements that must be in place for meeting this rule for the protection of personal health information their organizations maintain, create, transmit, or store. After completing this course, a healthcare provider will have a clear understanding for what needs to be place when it comes to meeting these HIPAA requirements for medical records.