Navigating the maze of changes with Form 5500
Cathleen M. Hampton
90 Min
Product Id: 704588
This webinar will discuss practical information to ensure compliance with the myriad of changes made to Form 5500 filing requirements. The Instructor will discuss EFAST2 processes and Schedule C disclosures and review changes to the 2014 Form 5500 series reports and 2015 Form 5500-SUP draft instructions. Participants will understand audit requirements and how to handle late deposits.
CMS Hospital CoP and TJC Telemedicine Standards, Telemedicine Credentialing and Privileging
Sue Dill Calloway
2 hrs
Product Id: 705491
This webinar will give insights on regulations and CMS interpretive guidelines which are now part of the hospital CoPs on telemedicine credentialing. It will discuss CMS mechanism for all hospitals to use proxy credentialing with Medicare-certified hospitals or other telemedicine entities. It will further discuss why written agreement is required, and insights on the requirements in the written agreement. It will also provide insights on standards, Joint Commission has on telemedicine in the leadership chapter.
How to Transition from Paper to Electronic Records in a Regulatory Environment
Charlie Sodano
75 Min
Product Id: 703576
This webinar will cover effective and efficient ways to transition from paper to electronic records in a regulated environment. It will address compliance issues, complexity in decision making and implications specific to the pharmaceutical industry.
Credit card surcharging - who is going to do it and what are the stipulations for compliance?
Ray Graber
60 Min
Product Id: 702866
This training on credit card surcharges compliance will discuss how the recent changes in law will affect end-user organizations. It will also provide attendees with the tools necessary to review and deal with any potential surcharge/checkout fee situations.
Preparing Compliant eCTD Submissions: Are You Prepared for Upcoming FDA Mandate on e-Submissions?
Peggy Berry
60 Min
Product Id: 705349
This webinar will review the CTD format requirements including documentation and technical requirements for an eCTD submissions. It will help attendees prepare for implementing the FDA upcoming mandates on e-submissions.
Good Practices for Data Integrity, the new Guidance and one FDA Inspector's Experience
John R Godshalk
60 Min
Product Id: 704806
This webinar, by an ex-FDA, will cover Good Data Integrity Practice for GxP environments. Participants will understand what FDA looks for with regard to data integrity, what may need to be audited, the new guidance and application of data integrity, and relevant regulations for data integrity
Family Medical Leave Statutes for Small and Medium Business
Matthew W Burr
60 Min
Product Id: 705268
This training program will describe the scope, objective and domain of FMLA. It will help identify most frequent types of FMLA abuse and discuss case studies on FMLA abuses. The webinar instructor will also discuss best practices to carry out effective FMLA investigation and highlight documentation guidelines that will help your company stay out of court and avoid settling claims.
Practical Risk Appetite and Risk Tolerance
Mario Mosse
90 Min
Product Id: 704949
This webinar will discuss how to implement and monitor risk policy. The instructor will explain the challenges and opportunities involved in developing and implementing an effective risk appetite statement, which is supported by risk limits, and the determination of actual exposure against those limits and risk tolerance.
How to Conduct a HIPAA Risk Assessment
Brian Tuttle
60 Min
Product Id: 704592
This training program will cover the proper methodologies of conducting a HIPAA risk assessment based on the formula used by federal auditors and based on the NIST (National Institute of Standard for Technologies) guidelines. The session will also cover the most important aspects to be aware of in terms of the federal auditing process as well as the new risks regarding patients suing for wrongful disclosures.
Patients Suing Under HIPAA
Brian Tuttle
60 Min
Product Id: 704387
This training program will be addressing major changes under the Omnibus Rule which give patients the right to sue under state law citing HIPAA. There are enormous issues and risks for covered entities and business associates under Omnibus.
US Expatriate Compensation Planning and Reporting Methodology
Matthew W Burr
60 Min
Product Id: 705362
This webinar will offer attendees an understanding of compensation and planning for U.S. expatriates. It will assist you in preparing compensation plans, the reporting process, and in reporting expectations. The training session will also discuss variations across countries and common concerns/mistakes.
Developing Effective Workers Compensation Case Management Strategies
Joe Keenan
90 Min
Product Id: 705315
Workplace injuries and illnesses can cause huge financial tolls and disrupt the workforce in an organization. This webinar will dive into the importance of developing an effective Return to Work program and presenting the program to senior management.
System Suitability Testing (SST) for USP and FDA Compliance
Dr. Ludwig Huber
75 Min
Product Id: 702512
Amid several other critical discussions, this training program will detail FDA and international requirements for system suitability testing; SST in comparison with equipment qualification and quality control sample analysis; critical parameters for SST in EP and USP; recommendations for implementing the updated <621>; and developing an SOP for system testing.
How to Perform a HIPAA Risk Assessment
James B Wener
60 Min
Product Id: 704058
This risk assessment training will discuss why it is essential to perform a risk assessment and what kind of breaches can occur. It will also list what HIPAA regulations require and what it should tell you.
Setting Specifications for Drug Substances and Drug Products
Peggy Berry
90 Min
Product Id: 704859
This 90-minute training will discuss the requirements of ICH for using testing and stability data to set specifications for drug substances and drug products including use of special stability studies. Attendees will also learn the requirements for changing specifications through the lifecycle of the product.
HIPAA Training for Security Officers
Brian Tuttle
60 Min
Product Id: 704350
This webinar will be addressing how practice/business managers (or compliance offers) need to get their HIPAA house in order before the imminent audits occur. It will also address major changes under the Omnibus Rule and any other applicable updates for 2018. The primary goal is to ensure everyone is well educated on what is myth and what is reality with this law, there is so much misleading information all over regarding the do’s and don’ts with HIPAA.
Understanding HIPAA Security Rule Requirements
Jay Hodes
60 Min
Product Id: 704877
This webinar will teach you all the requirements that must be in place for the HIPAA Security Rule and how to demonstrate compliance with all the required and addressable safeguards. After completing this course, a Covered Entity or Business Associate will be able to know what needs to be place when it comes to all of the HIPAA regulations.
The Good, the Bad & the Ugly : A ‘How-to’ guide on Employee Performance Management - Module 3
Wes Pruett
90 Min
Product Id: 704747
This training program will highlight the steps for conducting disciplinary investigations. It will discuss how to hold employees accountable for sustained change and detail a simple system for determining how to coach employees. It will also focus on Performance Improvement Plans (PIPs) and how progressive discipline policies can hurt you.
Form I-9 and E-Verify, Getting and Staying Compliant
Cathleen M. Hampton
120 Min
Product Id: 703756
Today, in order to avoid astronomical fines for non-compliance, employers need to be ever so vigilant and diligent in their process. This webinar discussion will include a review of the penalties ICE and Office of Special Counsel (OSC) can impose. Additionally, the webinar will review paper versus electronic I-9 forms and the common mistakes employers make in the process.
Export Documentation and Procedure
Iliyana Hristev
90 Min
Product Id: 704537
This webinar training will discuss the export documentation and procedures. The instructor will discuss the differences in documentation requirements between exporting and domestic business , how to create important documentation including commercial invoice, shipper's letter of instruction, customs and consular invoices, product specification documentation and certificates of origin







