Compliance Training Webinars for Regulated Industries

Learn the basic overview of the international medical device Quality Management System -- EU’s Quality Management System under ISO 13485:2016. Implementation, training requirements, content and annual internal audit / inspection expectations.

This webinar on Estimating Reliability Performance of products will show how you can use Accelerated Life Testing methods (ALT) to reduce costs, minimize risks and ensure adequate product performance prior to launch.

In this webinar, get step-by-step instructions on creating your 2020 strategy utilizing agile principles. It is a simple straightforward process you and your team can execute with ease. Begin with a 360-degree analysis of your stakeholders, high light priorities, align to the larger organization goals, identify risks & roadblocks, create meaningful measurements, and develop the 2020 roadmap.

Attend this webinar to understand in detail Safety Hazards with specific emphasis on Hazard Recognition and Response and putting in place critical Written Programs and Employee Training to address.

This IRS form 990 webinar will discuss how to fill core Form 990, the complex elements of the form, the governance/insider compensation rules for exempt status , current areas of IRS focus and exam activity, how to avoid common mistakes that can increase your organization’s audit risk, best practices to consider in return preparation, and how the story your Form 990 is telling about your organization.

In this course you will discover how to navigate relationships you find challenging.You’ll be oriented to an approach with clear steps on what -and what not- to do.You’ll learn a realistic approach that teaches you the skills necessary to navigate your challenging relationships with clarity, confidence and ease! An approach that works!

In this webinar attendees will learn the new NLRB changes on employee handbooks, how to update your employee handbooks and what policies must be added to employee handbooks for 2019 to reduce your company’s risk and help you mitigate the numerous workplace regulations that can impact your company.

In this paid sick leave and family leave webinar, learn the upcoming updates related to – legal PTO policy, carryover and notice/posting requirements, PTO leave with protected leave under FMLA, PTO accrual rates, PTO and the exempt employee, pregnancy disability leave, caps on vacation banks.

In recognition of the challenges associated with the execution of international payment terms, this webinar will provide both importers and exporters with the insight necessary to make well-informed credit decisions. The webinar uses a combination of easy-to-understand explanations and real-life scenarios, ideal to credit managers, international salespeople, logisticians and order management personnel.

This seminar will explore the unique and critical relationship between regulatory compliance, compliance documentation, and technical operations training and improved performance, standardization and world class regulatory compliance. We will also discuss the area of training in regulated environments, its importance, and its relationship to compliance documentation.

This webinar will discuss employers’ rights and obligations with respect to employees’ use of legalized marijuana for medicinal or recreational use. With a number of states legalizing either or both type of use, employers must keep on top of the current trends, especially in light of the fact that marijuana is still a controlled substance under federal law.

This FDA audit webinar will highlight the purpose of FDA audits and scope, Understanding of QSIT audit and how to develop an audit preparedness plan. It will also give understanding of what the FDA will look for at the conclusion of your audit and how to communicate with FDA before and after the audit.

In this webinar, we will review in detail major considerations to be well-thought-out during the prescription drug product development process. We will review in depth FDA cGMPs and their importance in drug manufacturing. We will review the submission process and post-approval commitments. This webinar is Part 2 of a 2 Part series.

Attend this webinar to understand the definitions of in-house IVDs, the regulatory requirements including classification & essential principles, the NATA requirements related to how and when IVDs can be used as a research or diagnostic tool and the current laboratory supervision requirements for the ability to perform and report on in house IVDs.

Attend this webinar to learn how to create a GMP compliant training program and avoid human errors when implementing/improving a training program. It will discuss important elements like curricula, training management systems, training effectiveness and more.

This training program will highlight common issues that occur over time with material compliance programs, and demonstrate how to address them. This can result in a more effective and responsive material compliance effort for your company.

The International Standards Organization (ISO) defined the ISO 26000 guideline for the use and planning of all structured, measured, and monitored social responsibility programming. This standard enables companies to initiate and track performance of CSR programs by focusing on the triple bottom line (TBL) - people, planet, and profit. This training program will offer in depth look at the key components of the ISO 26000 guideline and best practices to implement and support a social responsibility program.

The webinar covers the need for understanding the ISF 10+2, 10+5 and its processes. The reason for filing the ISF, when to file the ISF and who files the ISF.

This webinar will review in depth FDA and other important US Regulatory Bodies roles and responsibilities pertaining to the prescription drug development process. We will explore the recognized regulatory approval pathways, good clinical practice and clinical study concerns.

In this webinar, get an overview of auditing for microbiological aspects of pharmaceutical and biopharmaceutical manufacturing. It will cover pertaining regulations and their applications to provide success when being reviewed by an auditor.