Compliance Training Webinars for Regulated Industries

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.

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.

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.

This webinar will discuss current medical device registration requirements in Brazil and recent regulatory changes. Topics to be discussed are Company Licensing, risk assessment, how to get regulatory clearance,GMP certification, INMETRO certification, govt fees etc.

This Method validation protocol training will discuss the regulatory requirements of analytical test methods, the USP good documentation practices <1029> and how to establish acceptance criteria for validation.

This webinar will discuss the new content of revised USP chapter 1058, will compare with the old version and discuss how to implement it. The approaches for risk based qualification, instrument lifecycle, quality agreements, how to integrate software validation and equipment qualification, how to integrate with GAMP Guide on Laboratory Computerized Systems.

Excel has many built-in functions that help you deal with that data. Attend this webinar to learn how to turn the data into meaningful information and then provide the answers that you need for yourself, your boss, your company or your organization. Learn how to use performance reports, scenarios, use of Excel in multi-user environments, relative and absolute formulas and many more.

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.

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.

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.

This AML compliance webinar will discuss recent developments in Bank Secrecy Act including various forms such as Currency Transaction Report (CTR), money log and Suspicious Activity Report (SAR).Attendees will learn best practices to ensure compliance with BSA regulations and avoid violations and fines.

This GDPR webinar will discuss the benefits, the procedure of implementing ISO/IEC 27001 standard compliant with an ISMS deployment for GDPR compliance and discuss how to determine primary data breach risks and incident handling as per GDPR mandates.

This SQM webinar will discuss how to establish a Supplier Quality Management program from selection to approval, the ON-going maintenance and disqualification of suppliers will be explored through definition of supplier classifications. How to build risk management into the process will be discussed. The webinar will explore the use of Quality Agreements to manage suppliers.

This course on 510K documentation for software or software enabled device will detail what Medical Device companies need to know what Software Specific documentation needs to be prepared for successful 510K submittals to avoid delays or denial of the 510K approval. it will discuss key to comply with IEC62304, FDA guidance with in software development and verification/validation process.

This CAPA evaluation, implementation and integration webinar will discuss FDA regulatory requirements, how to evaluate your CAPA system, how to integrate with QMS and the best practices approach to initiation, evaluation and implementation of CAPA system along with discussion about CAPA documentation requirements.

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.

In this Water System Webinar the author will explain the process he uses as a consultant for investigating and solving water system or product contamination problems with water organisms. Case studies of real life problems he has resolved will be presented to illustrate the process.

In this webinar the presenter will review the known and anticipated 2019 MIPS requirements for 2019 at a detailed level. It will also address how the Bipartisan Budget Act of 2018 will impact planning and performance in the MIPS in 2019. Discussion will be on the best practices for performance in each of the 4 MIPS performance categories at a granular level, including quality measure selection, implementation and performance tracking, strategies designed to obtain 100% scores on the Promoting Interoperability (formerly Advancing Clinical Information) and Improvement Activity categories, and optimizing performance in the Cost category of MIPS.

This OSHA 300 log recordkeeping webinar will discuss the new injury recordkeeping E-submission rule requirements & a basic review of recordkeeping in terms of site specific case scenarios will be presented.

This webinar will discuss the fundamentals requirements for system which gets audited during FDA inspection and how to conduct internal audit, report writing and audit follow ups.