Compliance Training Webinars for Regulated Industries

This 3-hr virtual seminar on Project Management in Human Resources will focus on key project management skills for the HR professional. You will learn proven, successful techniques for detailed, systematic, team-involved planning and effective implementation.

The course is designed to review critical elements of the new regulations and will be run as an interactive 2 hour course designed for business leaders with a good working knowledge of current requirements.

This webinar will provide participants with competitive insight into differences between states’ regulatory agencies, impact(s) of states’ funding sources on their food regulatory authority and variations in states’ history of adopting federal food policies such as FDA Food Code.

This course will lead employers and their legal teams in responding to charges and complaints filed by the National Labor Relations Board. Greg will also discuss about Unfair Labor Practices, Information requests, Terminations, Section 8(a)(1), Section 8(a)(3) and Section 8(a)(5).

This course will discuss the interface between archeology and engineering. This includes land surveying and location surveying; support facilities for archeological digs. This course also discusses the interface between engineering and local history.

This FASB revenue recognition standard webinar will discuss the various steps involved in this standard and also the technical guidance to prepare a revenue recognition model.

This equipment cleaning validation webinar will explain cleaning validation program steps, cleaning agents selection, documentation, cleaning method set up and how to reproduce cleaning validation program and various simple but powerful tools for achieving an in-depth Cleaning Validation Program, and continuous monitoring that meets FDA expectations.

Learn how to create a dynamic budget spreadsheets by using various techniques – streamline & preserve formula , how to create both operating and cash flow budget, how to improve integrity of spreadsheet using VLOOKUP, Excel’s CHOOSE, SUMIF, ROUNDUP and ROUNDDOWN worksheet functions.

This session will discuss enterprise-wide stress testing program, the complexity of CCAR, A state of the art review of CCAR stress test design, CCAR frameworks, Organizing and validating the transmission chain from macro to market shocks down to single position shocks and how to balance art and science in stress test design.

This GMP training will elucidate the key elements of world class QA and compliance practices specifically for animal health manufacturing companies. These practices support a robust quality system, ensure the firm’s quality standards remain current, and inform the GMP auditing and training processes.

The OSHA Voluntary Protection Program (VPP) is the highest award in Health and Safety Excellence that OSHA presents to an organization. This training program will guide attendees with best practices in implementing the OSHA VPP program. It will offer a broad overview of how to work with OSHA to achieve VPP site implementation success.

This health Reforms training will examine where U.S. health reform now stands in light of recent legislative and administrative changes, the outlook for additional policy initiatives in 2018 along with their market impact on payers and providers, and who will be the principal industry winners and losers in the ever changing health reform environment.

In this revised ICH GCP guideline on budgeting and contracts for clinical trial webinar will discuss the impact of changes in ICH GCP E6 R2 on investigator, site, sponsors CROs roles and responsibilities and the impact of clinical trial conducts and organizational practices along with evaluate solutions/applicability/modifications of organizational SOPs, processes, procedures and staff training; and discuss opportunities for implementing the revised guideline.

This FDA communication best practices webinar will discuss the best practices for communication with FDA staff, general timing of communications, how to deal with deficiencies and key resources for premarket applications and post market communications.

This virtual seminar on Family Care and Medical Leave in California will examine the requirements for family care and medical leave, employers covered by the CFRA/FMLA, a covered employer’s duty to post notice of CFRA requirements and obligations, employees eligible for CFRA/FMLA leave, and more. The program will also explore the interplay between California’s Pregnancy Disability Leave law, CFRA/FMLA, compensation while on leave, continuation of benefits while on leave, employer’s prohibited actions under the CFRA, employee’s return to work policies, and more.

Understand the definition of New York State paid family leave and how it will impact your organization. The webinar will also discuss the process for filing, pending changes, and its association with the FMLA.

This Medical device complaints handling webinar will discuss the best practices of complaint handling and how to include it in your CAPA program and how to apply risk management to the complaint handling system.

In this Dietary supplements batch control webinar learn what and how to create master manufacturing records, what batch production records to create and what to do with completed batch records as per FDA 21 CFR Part 111 requirements. Learn inventory management techniques that make the creation and management of Master and Batch production records easier.

This webinar will teach attendees best practices for building a sustainable vendor qualification program for FDA regulated industries. It will discuss common pitfalls to avoid when qualifying vendors.

This webinar will discuss the CMS requirements for standing orders and protocols in four separate sections. It will describe that all protocols must be approved by the Medical Staff even if the protocols are department specific.