Compliance Training Webinars for Regulated Industries

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 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.

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.

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.

This webinar will address HIPAA regulations from a different perspective - from the perspective of the person in charge of moving an organization or facility toward full compliance with HIPAA – the HIPAA Security/Privacy Officer.

Buying software is a fact of life for most companies. There is fierce competition in the market, with multiple software vendors trying to convince to buy their product. How do you determine whether to buy the software or having it built in house? Or which vendor to choose? And if you buy something, how do you determine whether to have it hosted? And are there any regulations that apply to this software? And if so, what are they?

This training program will highlight exempt versus nonexempt classification of employees for compliance with federal overtime laws. It will include best practices and practical steps to ensure lawful classifications.

This training program will discuss why an effective export control program (ECP) consists of many processes that connect, intersect, and overlap. It is vital that employees responsible for export compliance know the requirements of Title 15, CFR, Part 30, and the responsibilities of U.S. parties at the time of export. This online training will provide compliance materials that examine U.S. Customs and Border Protection regulations for the international logistic arena.

This training program will discuss why an effective export control program (ECP) consists of many processes that connect, intersect, and overlap. It is vital that employees responsible for export compliance know the requirements of Title 15, CFR, Part 30, and the responsibilities of U.S. parties at the time of export. This online training will provide compliance materials that examine U.S. Customs and Border Protection regulations for the international logistic arena.

This webinar will discuss the principles of drop shipment exemption. It will also detail how you can help your company legally avoid tax assessments by your drop shippers on your resale orders.

This training program will help attendees to learn the efficient and time-tested way to conduct an OSHA audit of their facility and then what to do with it!. Attendees will also learn the OSHA hazards and how to avoid those hazards.