WEBINARS

 

Compliance Training Webinars for Regulated Industries

How to Go from Pivot Tables to Dashboards Using Excel

webinar-speaker   Joe Weil

webinar-time   90 Min

Product Id: 705599

This webinar will update your Excel skills by teaching you how to create impressive Dashboards even if you don’t have artistic talent. At the conclusion of this webinar you'll be able to create amazing, interactive Excel dashboards that update at the click of a button and leave a lasting 'wow' impression.

Recording Available

* Per Attendee $229

 

Addressing Non-Conformances using Root Cause Analysis (RCA)

webinar-speaker   Michael Brodsky

webinar-time   60 Min

Product Id: 704861

In this webinar you will learn how to determine the Root Cause origin of a problem. You will learn a specific set of steps, with associated tools, to find the primary cause of the problem, so that you can prevent occurrences.

Recording Available

* Per Attendee $249

 

Good Documentation Guideline (Chapter <1029> USP)

webinar-speaker   Dr. Afsaneh Motamed Khorasani

webinar-time   60 Min

Product Id: 705130

This webinar will familiarize participants with USP Chapter <1029> on good documentation guidelines. This session will wrap up the general concept and will provide information as to what needs to be documented in certain records.

Recording Available

* Per Attendee $299

 

Navigating California Prop 65 Incorporating FSMA Preventative Controls, Best Practice Approach

webinar-speaker   Gina Reo

webinar-time   60 Min

Product Id: 706263

Attention Food Manufacturers, attend this webinar to learn latest FSMA based strategies to navigate the complexity under Prop 65. Prop 65 is an ever-changing regulatory arena, with complex requirements, frequent legal actions and strict labeling and notification regulations.

Recording Available

* Per Attendee $229

 

The Equal Employment Opportunity Commission: Mission, Claim Filing, EE & ER Responsibilities

webinar-speaker   Diane L Dee

webinar-time   120 Min

Product Id: 706797

Given that every complaint has the potential to become a lawsuit, employers should investigate every case in a manner in which it can be presented to a court of law, if necessary. As potentially disruptive as investigations can be, they must be prompt, thorough and effective to ensure all parties’ protection.

Recording Available

 

Interdisciplinary Bedside Rounds: The State of the Art

webinar-speaker   Toni Cesta

webinar-time   60 Min

Product Id: 705237

This webinar will identify the key stakeholders needed for effective interdisciplinary rounds. It will review the best practice rounding processes including scripting and time management.

Recording Available

* Per Attendee $249

 

Design Control for Medical Devices: Overview and Design Inputs

webinar-speaker   Alan M Golden

webinar-time   60 Min

Product Id: 706618

Overview of Design Control for Medical Devices, with an emphasis on design inputs. Seminar will go over regulations, basic concepts in design control and importance of design inputs and how to write appropriate inputs.

Recording Available

 

IT Auditing: How to Apply Analytical Procedures for Meaningful Analysis

webinar-speaker   Robert Davis

webinar-time   60 Min

Product Id: 706680

This webinar facilitates understanding analytical procedures associated with performing IT assurance services and defining risk areas using a system perspective. The "IT Auditing: How to Apply Analytical Procedures for Meaningful Analysis" webinar presents guidance following the general structure of planning, studying, testing, reporting, and follow-up. The offered activities apply to broadly or narrowly defined IT audits.

Recording Available

* Per Attendee $229

 

21 CFR Part 11 and QMS Software Risk-Based Implementation

webinar-speaker   John E Lincoln

webinar-time   60 Min

Product Id: 706363

CGMP-compliant companies must develop / implement formal software controls and usage, starting with proper verification and validation methods. This is an important consideration for a company’s Quality Management System (QMS) and must consider applicable elements of electronic records / signatures / Part 11. The US FDA recently added data integrity and cybersecurity to these requirements. These activities must be properly documented.

Recording Available

* Per Attendee $299

 

Anti-Kickback, Fraud, Stark, and Marketing - Where are the Landmines?

webinar-speaker   William Mack Copeland

webinar-time   90 Min

Product Id: 704950

This webinar will provide an in-depth understanding of the Federal False Claims Act, Federal Anti-Kickback and Stark laws, and discuss how marketing activities can trigger either or both.

Recording Available

* Per Attendee $299

 

Human Error and Cognitive Load: How to Reduce Memory and Attention Failures

webinar-speaker   Ginette M Collazo

webinar-time   60 Min

Product Id: 704210

This training program will discuss the types of human error, the taxonomy of human error, human error reduction initiatives, individual performance, cognitive load and human error, cognitive load categories, and more.

Recording Available

* Per Attendee $299

 

Basic Cleanroom Technology, Operation and Contamination Control in a Nutshell

webinar-speaker   Charity Ogunsanya

webinar-time   90 Min

Product Id: 706142

Attend this webinar to understand the Clean Room regulations, design, classification, sources and types of particles. Learn how to create a common ground between these varying regulations and requirements. It will discuss the types of micro-organisms, routine monitoring processes, and typical mitigation steps to effective contamination control.

Recording Available

* Per Attendee $299

 

Bank Compliance Failures: Examples and Lessons

webinar-speaker   Jim George

webinar-time   60 Min

Product Id: 706784

This webinar uses actual case studies to look at what leads to compliance failures, and how to handle them. In each case. What were the specifics of the situation? Why was there a failure? How was it identified? What did it take to fix it? How could it have been avoided? (Lessons learned). It concludes with a summary of the evident patterns and learnings.

Recording Available

 

Risk-based Design Control - The New Paradigm for Medical Device Design

webinar-speaker   Jose Mora

webinar-time   60 Min

Product Id: 706095

In this webinar, learn about the 2019 approach to compliant design control, how to create, manage, and maintain the information found in the various Risk Management documents and files. Get insights about how to shrink documentation time to provide enough time for actual risk management and mitigation.

Recording Available

* Per Attendee $299

 

Understanding and Responding to Bribery & Corruption Red Flags

webinar-speaker   Stanley Epstein

webinar-time   90 Min

Product Id: 706782

Corruption is a form of dishonesty or a criminal offense, undertaken by a person, or an organization entrusted with a position of authority, in order to acquire illegal benefits or abuse power for one's private gain. Corruption may involve many activities, which include bribery and embezzlement, and it may also involve practices which are still legal in many countries. “Red-flags” provide a warning that illegal activity may be taking place.

Recording Available

* Per Attendee $249

 

Computer Fraud and Countermeasures

webinar-speaker   Richard Cascarino

webinar-time   60 Min

Product Id: 706783

This webinar is intended to raise auditors’ abilities within the sphere of forensic auditing through a combination of lecture and case-study.

Recording Available

 

BSA/AML Contextual Awareness of High Risk Customers

webinar-speaker   Doug Keipper

webinar-time   60 Min

Product Id: 705472

This webinar will highlight the steps to identify and evaluate high-risk customers. Learn how to perform BSA, AML risk assessments.

Recording Available

* Per Attendee $229

 

Establishing a Robust Supplier Management Program

webinar-speaker   Kelly Thomas

webinar-time   90 Min

Product Id: 706055

This course will review regulatory guidance governing Suppliers and the elements of a robust supplier management program including, initial qualification, supplier performance monitoring, and scorecards, supplier audit options, and quality agreement requirements. It will discuss how to utilize risk-based quality tools to determine supplier classification with a risk assessment example. Recent FDA audit findings will also be reviewed.

Recording Available

* Per Attendee $299

 

Automating Excel: An Introduction to VBA

webinar-speaker   Mike Thomas

webinar-time   90 Min

Product Id: 705075

This Excel webinar gets you started with VBA. It's aimed at advanced users of Excel, with little or no programming experience, who wish to take their level of automation knowledge beyond the macro recorder.

Recording Available

* Per Attendee $179

 

Auditing the Human Resource Function

webinar-speaker   Matthew W Burr

webinar-time   60 Min

Product Id: 700648

This webinar will cover auditing human resources practices for compliance and liability to help identify and correct any areas that may not comply with applicable laws and/or do not comply with company policy.

Recording Available

* Per Attendee $229

 

 

 

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