Risk Areas Planned for Review and Regulatory Changes - New Challenges With Respect to Government Audits and Investigations in Health Care
Susan Lee Walberg
60 Min
Product Id: 703322
This webinar will focus on the current healthcare fraud and abuse enforcement environment and the specific emerging risk areas and strategies for dealing with those. Attendees will learn how to best use their existing resources and data to stay ahead of these government audits and investigations.
Updating HIPAA Compliance in Medical Offices
Jim Sheldon-Dean
90 Min
Product Id: 703330
This HIPAA compliance training will focus on the privacy policies and Notices of Privacy Practices that must be updated to ensure compliance with the final HIPAA Omnibus rule. Attendees will learn best practices to avoid breaches and penalties for non-compliance.
Managing Export Authorizations during the ECR Transition Period: How to Maximize Efficiency While Minimizing Risk
Darrell Coleman
60 Min
Product Id: 703311
This webinar will explain how to manage export authorizations during the transition of products to the Export Administration Regulations (EAR). It will discuss advantages and disadvantages associated with transitioning products as well as the various exceptions available including the STA exception for the new 600 Series products.
Why Social Networking Is a Concern for Human Resource Professional: Complying with Employment and Labor Laws
Susan Fahey Desmond
90 Min
Product Id: 701872
Understand why social networking sites use by employees is a concern, the potential legal risks associated with use of social networking sites for recruiting process, and how your failure to handle a social networking problem can lead to other legal problems.
Essential Do's and Don'ts for Navigating a Successful 505(b)(2) Drug Application
Thomas Reilly
60 Min
Product Id: 703314
This FDA New Drug Approval process training will provide attendees with the knowledge and skills needed to develop a successful 505 (b)(2) program.
Understanding and Interpreting the EMA Reflection Paper on GCP Compliance in Relation to Trial Master Files (paper and/or electronic) for Management, Audit and Inspection of Clinical Trials
Eldin Rammell
60 Min
Product Id: 703281
This training will give attendees an insight into the interpretation of GCP regulations by the European Medicines Agency (EMA) as they relate to the management of trial documents, focusing especially on clarification within the paper on disputed and ambiguous areas of trial master file (TMF) management.
Enterprise Risk Management (ERM) - Implementing a Practical and Effective Solution, and Making ERM Part of the Fabric of Your Organization
Robert Brewer
75 Min
Product Id: 703309
This webinar will discuss how to implement an effective Enterprise Risk Management (ERM) program in your organization. Attendees will learn best practices for developing a successful and sustainable risk management process.
Stress-Testing for Financial Institutions, Beyond Regulatory Constraints
Fred Vacelet
90 Min
Product Id: 703327
This financial risk management training will teach attendees how to participate in stress-testing initiatives and communicate results. Attendees will learn the tools and techniques to manage their institution’s financial risk.
7 Pillars of an Effective Compliance Program for Healthcare Companies: Lessons Learned from a Prosecutor's Perspective
Alice H Martin,Michael Rosen
60 Min
Product Id: 703280
This healthcare best practices training will discuss the seven recognized pillars that a compliance plan should include and the details that will allow attendees to reduce their company’s potential liability under the Federal U.S. Sentencing Guidelines. Learn from examples of healthcare companies that did not have or follow an effective compliance plan and the resulting civil fines and penalties as well as government oversight and audits that ensued.
Social Media and Marketing FDA Regulated Products
Mukesh Kumar
60 Min
Product Id: 702233
The webinar will discuss the do’s and don’ts for using social media in marketing FDA-regulated products. Common issues, misconceptions, perceptions, and possible solutions will be discussed. The presentation will to familiarize you with the current FDA rules and help you plan for developments expected in the near future.
3 Ways to Avoid Costly Wage and Hour Problems
Michael Haberman
60 Min
Product Id: 703293
This Fair Labor Standards Act compliance training will focus on the ways to avoid costly wage and hour problems under FLSA. Attendees will learn exempt classification and how to calculate overtime.
Illegal Harassment v/s Legal Workplace Bullying
Catherine Mattice Zundel
60 Min
Product Id: 703291
This training will help you understand the concept of workplace bullying. You will understand the similarities and differences between illegal harassment with legal workplace bullying & how to handle them. Attendees will learn tools for managing bullying at work.
Risk Aware Intelligence - Recognize Potentially Overlooked ERM Risk Identification Blind Spots
Jason Ackerman
60 Min
Product Id: 703296
This Enterprise Risk Management (ERM) training will help attendees learn an innovative approach for integrating ERM risk assessment, crisis management, and business continuity. Attendees will leverage this approach to think strategically about potential risk identification blind spots and simultaneously evaluate day-to-day operating assumptions that can preserve value and enhance process maturity.
Performing an OIG (Office of Inspector General) Excluded Provider Audit
Kevin McPoyle
90 Min
Product Id: 703276
This training on healthcare compliance will teach the attendees best practices for conducting a self audit of excluded providers. Learn how to prepare and conduct an audit to ensure compliance with this important mandate of Medicare participation.
Cosmetics - How Are they Regulated?
Susan Augello-Vaisey
60 Min
Product Id: 702311
This webinar will provide a comprehensive overview of FDA regulations for cosmetic products. It will help you understand how to be compliant in manufacturing, labeling and advertising of cosmetic products, and thereby ensure successful FDA and state inspections.
How To Translate Academic and Discovery Assays Into GLP Compliant Assays
Todd Graham
60 Min
Product Id: 703275
This GLP compliant assay training will help attendees deal with the challenges and pitfalls that may occur when translating assays as demonstrated in the scientific literature or through internal discovery efforts.
Annual Risk Assessment (ARA) - Keys to Maximize the value of an Internal Audit Department
Robert Brewer
75 Min
Product Id: 703297
This webinar will cover how to have an effective Annual Risk Assessment (ARA) and internal audit’s role in ARA. You will be able to identify the appropriate risk framework, their risk rankings, and balancing their available resources.
Foreign Corrupt Practices Act (FCPA) Webinar
Jon Groetzinger
60 Min
Product Id: 701771
In this Foreign Corrupt Practices Act (FCPA) webinar training understand the prohibited and exempted actions as per FCPA act, how to find the non compliance issues and how to implement FCPA compliance policies and procedures in your organization.
Basel III – What's new vs. Basel II
Varun Agarwal
90 Min
Product Id: 703273
This Basel III training will focus on the key aspects of Basel III and highlight how it differs from those in Basel II. It will discuss additional compliance requirements for Basel III, the costs involved, implementation timelines and provide a framework for end-to-end implementation.
3-hr Virtual Seminar: FDA's Establishment Registration and Product Listing Requirements, User Fees, Fee Waivers and Market Exclusivity
Karl M. Nobert
3 hrs
Product Id: 703269
This 3-hour training will review and compare FDA’s Establishment Registration and Product Listing Requirements; and available User Fees, Fee Waivers and Marketing Exclusivity for Drugs, Biologics, Medical Devices, Food, Tobacco and Animal Health Products.