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Courses

  • 21 Request Info

    The Often-Forgot Human Side of Project Management

    Overview: This webinar gives you the fundamentals of effective project management with an emphasis on the "human side".
  • 22 Request Info

    What Questions Employees are asking on the Internet

    Overview: Learn what employees are researching on the internet about workplace conditions, management, employment law, and what employers can do and restrictions that are in place. Why you should Attend: Participants should attend this webinar if they are new to HR or are new to management and supervision. Areas Covered in the Session: What boundaries employers should consider setting Avoid the risks of miscommunication Policies and procedures employers can implement and more
  • 23 Request Info

    How to Document Employee Discussions and Why that is Important

    Overview: Documentation is both the bane and the blessing for HR. It is difficult to get people to do it, but it is preferred by attorneys and believed by judges and juries.
  • 24 Request Info

    Difference Between Mentor, Coach, and Manager in Motivating Employees to High Performance

    Overview: Learn the different skills to Mentor, Coach, and Manager Learn the role of a Mentor, Coach and Manager in team engagement and employee loyalty. Successful career management by employees means accountability and getting formal and informal feedback. Talented human capital will be the prime ingredient of "business success"in the future. Organizational culture that values mentorship and coaching and includes constructive and timely feedback.
  • 25 Request Info

    Online course on Your Employees are Organizing a Union

    Overview Managers and Supervisors are taken to task everyday in managing their Non represented employees. It is important for them to learn the Initial warning signs of Union Organizing long before a Union gets the appropriate number of signed Authorization Cards and the NLRB Conducts a secret Election. Learn here the best Election is the one that is never held. This course will delve into the 20 + Initial Warning Signs of Union Organizing, What you Can Do and What you Cannot Do, Guidelines of Good Management, Dangers of Signing The Authorization Card, The NLRB Election, Unfair Labor Practices committed by Managers The information presented in this workshop will save costs. Event link : https://www.traininng.com/webinar/-201177live?channel=pharmavoice-JAN_2020_SEO Contact Info Traininng.com LLC Email: traininngdotcom@gmail.com Phone: US: (510) 962-8903 Phone: Zurich: +41 - 43 434 80 33 Website : https://www.traininng.com
  • 26 Request Info

    Critical Thinking, Problem Solving and Effective Decision Making

    Overview Many books have been written about creative problem solving. There is no easy way, no shortcut to becoming a first-rate problem solver. Develop solutions through an analytical approach Learn how to be able to identify relevant information that you can use to make decisions What makes a valid conclusion Use many perspectives to reach a conclusion This webinar gives you the tools to be able to identify your decision making style, andlearn to make better decisions through questioning, challenging assumptions, and seeing other's viewpoints.
  • 27 Request Info

    Dealing with Difficult People

    This webinar is filled with tips, techniques, strategies and tools that will make your dealings with difficult people much easier, You will learn how to diagnose exactly what the person is doing, Learn how to recognize what they are doing, and why that’s creating so much difficulty for you, and those around you, is the first step.
  • 28 Request Info

    Investigating a Complaint in the Workplace in the #MeToo Era

    Overview Conducting workplace investigations is one of the most challenging management and HR duties, but also one of the most important. This webinar is designed to train managers and HR professionals in how to conduct a thorough, emotionally sensitive and impartial workplace investigation. Complaints of sexual misconduct, harassment, bullying and abuse abound in today's workplace.
  • 29 Request Info

    Regulation E - The Basics and Error Resolution

    Overview Define Regulation E, what it is and who does this apply to in the ACH network and card world. Provide the meaning to Reg E terms such as consumer account and access device. List the steps involved in the Reg E error resolution process for electronic fund transfers (EFTs). Identify what happens when the consumer experiences the loss of a debit card (who’s responsible for what?). Illustrate examples of how to handle specific types of unauthorized transactions relative to Reg E. Describe when and to whom a specific party is liable (financial institution and/or consumer) by using specific examples.
  • 30 Request Info

    Your Employees are Organizing a Union

    By attending this webinar You will understand the "whys and where for" of the Union Organizer, their logic as to why they do and believe in what they do, The Webinar closes with a satirical presentation and discussion of "How to Ensure A Union in Your Workplace" ( "What you do not ever want to do in the Workplace").
  • 31 Request Info

    Organizational Change with Appreciative Inquiry

    Overview As a graduate student at Case Western University, Davide Cooperrider had access to study the organizational behavior at the renowned Cleveland Clinic.
  • 32 Request Info

    Make Your FDA Inspection as Painless as Possible

    In this session will be the limits of FDA's scope during an inspection, including what documents you are not required to show them, and the permissibility of photographs and affidavits. Without adequate preparation and cross-functional communication, it is difficult to manage a good FDA inspection. Your goal is to illustrate your firm is in substantial compliance with all regulations, but also to respond to the inspector's questions or concerns in a timely manner. This webinar will identify systems and processes, and recommended tactics, to make the inspection as painless as possible.
  • 33 Request Info

    Risk Management in Medical Device Design

    Overview: The webinar will explore the basic principles of risk management and planning as they relate to medical device design and as required by the FDA. It will present a logical process for risk management from risk identification through evaluation/rating and mitigation. Why should you Attend: The secret to preventing medical device recalls or at least to minimizing their impact is sound Risk/Hazard Analysis. Aside from being required, it is absolutely essential and necessary to the development and fielding of medical devices that offer a significant level of protection for patients and manufacturers alike.
  • 34 Request Info

    Fishbone Diagramming

    Overview: Fishbone Diagramming is an analytical approach used to identify and solve problems. Analysis is presented in the Seven Basic Tools of Quality in addition to advanced methods used to increase organizations effectiveness, efficiency and reliability. Specific areas presented: Look for Evidence The Post-it Exercise Pareto Chart Fish Bone Diagramming Process Reliability Modeling
  • 35 Request Info

    Acceptance Sampling Plans for Process Validation and Production Lot Monitoring

    Overview: Personnel involved in process validation and production control often rely on sampling methods to determine the suitability of a process before moving to production (process validation) or for checking production lots for acceptance. This webinar provides details regarding the generation of sampling plans that meet the desired statistical properties. By attending this webinar, participants will be able understand the key inputs and issues involved in determining acceptance sampling plans. Although software is generally used to generate sampling plans, the participants will gain useful insight into the methodology and its use in typical applications.
  • 36 Request Info

    3-Hour Virtual Seminar on The "New NAFTA": The USMCA

    Overview: The North America Free Trade Agreement (NAFTA) comprises Canada, the U.S. and Mexico, an agreement which has eliminated barriers to trade, promoted conditions of fair competition, increased investment opportunities, provided protection for intellectual property rights, and established procedures for the resolution of disputes. The United States-Mexico-Canada Agreement (USMCA), commonly referred to as the "New NAFTA,"is essentially NAFTA 2.0. The USMCA has been adjusted to include changes for automakers, stricter labor and environmental standards, intellectual property protections, and digital trade provisions.
  • 37 Request Info

    Equipment Validation, Tracking, Calibration and Preventive Maintenance

    Overview: FDA and EU regulations require that firms have a program for the calibration and maintenance of test and measurement equipment. The program must include: intervals, scheduling, specific procedures, limits of accuracy/precision, and remedial action in the event that the equipment does not meet established requirements. Prior to use, however, this equipment must be validated to make sure it produces product that meets its specifications. There are ways, though, to validate equipment already in use.
  • 38 Request Info

    Root Cause Analysis for CAPA - Myths, Challenges, and Best Practices

    Overview: This webinar will help you understand the critical ingredients for conducting an effective root cause analysis. You will learn about FDA expectations, tools and techniques, and tips for conducting and documenting root cause analysis. We will discuss the myths, challenges, and best practices for this critical process. We'll also cover the essentials of doing a failure investigation. Why should you Attend: CAPA is the cornerstone of quality improvement and it depends on an effective root cause analysis. Conducting an effective root cause analysis (RCA) can be a daunting task. And without a good root cause analysis, your CAPA will not result in the desired improvement.
  • 39 Request Info

    GMPs for APIs

    Overview: In this webinar we will discuss the regulatory expectations that apply to the production and control of active pharmaceutical ingredients. The discussion will start with the introduction of ICH Q7, the internationally accepted GMP for APIs, discuss the international regulatory and compliance issues associated with this GMP and each of the main areas of ICH Q7 to include: personnel, buildings and facilities, process equipment, documents and records, materials, production and production controls, packaging, and laboratory controls.
  • 40 Request Info

    Project Management for Non-Project Managers

    Overview: This webinar will address those project management critical tasks within each project phase that must be performed flawlessly for effective project execution to occur and will provide the foundation and direction for future study of the subject. Why should you Attend: It is not possible to present a complete treatment of project management in the span of 60-90 minutes. It is however possible to focus in on those most critical project management aspects that are critical to the success of any project. Without basic tools, it is not possible to effectively manage a project to the pre-determined end-date without turmoil and chaos.