Compliance Training Webinars for Regulated Industries

On June 30, 2016, the Department of Justice (DOJ) along with the Department of Homeland Security (DHS) have issued several rulings outlining several civil penalties increases, ranging from small hikes to doubling penalties. Not only does this ruling impact all immigration processes but it will impact the number of fines and penalties that employers must pay if they are audited for I9 documentation and impact most immigration processes and regulations. Learn the precise way to correct I9 documents to stay away from non-compliance and penalties.

This webinar will cover a number of common misperceptions about the Americans with Disabilities Act in the workplace. Employers must ensure that they are not making any of these mistakes when they interact with employees who have disabilities. Otherwise, they could be risking potential liability.

This OSHA Recordkeeping training will cover critical aspects of OSHA recordkeeping and its requirements, to be compliant with OSHA regulations.

This webinar will provide an overview of setting and maintaining specifications for Pharmaceutical and Biotechnology derived drug products throughout its shelf-life.

This webinar will help you to write clear, concise, and flexible SOPs. You will learn techniques for creating easy to read and clear SOPs your employees can easily follow. Well written SOPs ensure that your employees understand and consistently follow your manufacturing processes.

In this webinar attendees will learn the impurity and degradation product analyses tests on compounds of low concentrations for Identification and Quantitation. This webinar covers the approaches and the validation issues that must be met and maintained. Identifying and quantitating minor components is mandatory. The use of a valid approach with its backing by validation ensures that these analyses will be acceptable.

Given the global business environment, IT deployments are indispensable for enabling information reliability, processing efficiency, and communication expediency to acquire and maintain a competitive advantage. Because the information has measurable value, data collection, processing, storage, and transmission by organizational employees need appropriate safeguarding. Safeguarding information mandates addressing cybersecurity protection to ensure managerial due care and due diligence. Through Dr. Davis’ discussions, security professionals will acquire an appreciation for the complexities associated with ensuring an effective cybersecurity program.

In this webinar, learn how to develop an Allergen Control plan which is a critical component in your product safety initiatives. Understand how to implement, audit, enforce and update it continually.

In this webinar, learn to create flexible data queries that refresh when the data does. Create, then Pivot your report to fit your needs, filter your report with Excel’s Slicer tool, Target production delays, efficiency gains, scrap rates, key demographics and so much more from your data, Learn how the gurus in your organization analyze their data so quickly and become one too!

Join this webinar to learn approaches to setting up an internal complaint-handling system that ensures compliance with all GMP requirements.

This AML training will provide you the tools to identify the differences between money laundering and terrorist financing and how to protect your financial institute against potential criminal activity. It will also highlight the complexities of modern day proactive compliance departments.

In this webinar you will discover how you can resolve conflict situations early before they escalate into intractable disputes using proven responses and techniques that work. This webinar provides a practical road map for interpersonal conflict resolution in the workplace and beyond.

This webinar will address the red flags that may indicate money laundering and fraud in non-bank financial institutions. It will also provide guidelines for conducting enhanced due diligence (EDD).

Attend this webinar to get an overview of the Health Canada Medical Devices Regulations and its requirements. Also, get guidance on how to approach MDEL and Device Licensing, Renewals and Costs.

Attend this webinar to learn how to create and establish methodologies for gathering data, aggregating data, and for presenting results of data analysis. Also, get updated on the latest from financial regulators, Enterprise Risk think tanks and be introduced to best practices.

This training program will discuss how getting rid of the paper can increase your department’s efficiency and decrease overall long term costs. Some of these efforts will involve upfront costs or systems or your time to create and implement while others can be done immediately by taking advantage of improving technology offered by others. But even introducing just a few of them will reduce the paper in your department.

This webinar will describe the basic principles of pharmacokinetics, with specific emphasis on issues that can impact toxicokinetics in preclinical safety assessment studies. It will highlight methods for the optimization of physicochemical properties in the discovery and development of oral drug candidates and explore some of the preclinical methods used to select first in human (FIH) doses.

This 1-hr virtual webinar will give you the tools you need to maintain a quality supply of media and reagents in a variety of microbiology laboratories. A thorough understanding of the variety of challenges in maintaining quality media and reagents will be brought to the fore. This will allow you to perform microbiology testing with confidence.

In this webinar, you'll learn not only how to turn raw data into meaningful information but also how to present that data in a visually attractive way. This training will provide you with a solid foundation that you can use to build your own business reports.

This training program is intended for anyone directly or indirectly responsible for the creation, content or validation of CDISC data sets, tables, and data lists used to support research, drug or medical device efficacy and safety in a regulatory submission. Through case study analysis, the course will examine best practices to provide thoughts and ideas to develop or improve the CDISC mapping system.