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  • 141 Request Info

    Webinar on The Ancient Art of Listening

    Listening, truly listening and not merely being silent or politely waiting for your opportunity to speak or to correct the speaker, is among the hardest work you might ever do. But to truly listen completely so that you are not only hearing but processing what the speaker wanted you to hear and to learn, with your heart as well as with your brain takes practice. However, one must first be aware of this set of listening skills before one can begin to practice and then hopefully perfect one's ability to listen completely. This webinar will identify the proper environment, skills and techniques to assist the participant in continuing to develop and improve their ability in this most important and ancient of arts. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/The-Ancient-Art-of-Listening-508870/JANUARY-2018-ES-TRAININGREGISTRY
  • 142 Request Info

    Webinar on 7 Behaviors of Great Leaders

    All great leaders have common amongst themselves certain ingrained habits of behavior that help them separate from the pack and achieve at the highest levels. These habits are learned and developed in a very deliberate way. This webinar will delve into each behavior that is needed for you to be a great leader. This will include tools to help you assess yourself, develop and design a system of follow up to insure you continue to improve. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/7-Behaviors-of-Great-Leaders-506334/JANUARY-2018-ES-TRAININGREGISTRY
  • 143 Request Info

    Webinar on Employee Engagement: Keeping Your Workforce Motivated to Improve Results

    Do your employees jump out of bed each morning excited to come to work? When they’re at work are they totally absorbed in what they’re doing? According to a ton of research, the answer is, unfortunately, “probably not.”Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Employee-Engagement-Keeping-Your-Workforce-Motivated-to-Improve-Results-509532/JANUARY-2018-ES-TRAININGREGISTRY
  • 144 Request Info

    Webinar on Accounts Payable Internal Controls: How to Reduce Risk and Prevent Fraud

    Develop and Improve Internal Controls Based on COSO Frameworks to meet organizational objectives. This session by expert speaker Patrick Haggerty will cover organized approaches to the development of internal control systems and controls based on the COSO frameworks, including risk assessment, development of the control environment, training of employees and the objectives of the business. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Accounts-Payable-Internal-Controls-How-to-Reduce-Risk-and-Prevent-Fraud-508227/JANUARY-2018-ES-TRAININGREGISTRY
  • 145 Request Info

    Investigating Sterility Test Failures

    Sterility testing is widely used in both the medical device and pharmaceutical industries. The pharmacopeia test is the official procedure for testing the sterility of pharmaceutical products. Despite its importance and its widespread use, many people are not aware of the limitations of the sterility test and are unsure how to proceed when a failure investigation occurs. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Investigating-Sterility-Test-Failures-503878/JANUARY-2018-ES-TRAININGREGISTRY
  • 146 Request Info

    HIPAA Compliance Requirements | HIPAA Privacy Security 2018

    Being the HIPAA Security and Privacy Official involves not only ensuring you know the appropriate patient rights and controls on your uses and disclosures of protected health information, but you also have the proper policies and procedures in place. If audited or the subject of a breach investigation, you will be required to show the government you have all the necessary documentation in place for safeguarding patient Protected Health Information and indicate how you addressed all required security safeguards. This starts with the fundamentals of a HIPAA compliance program. Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901516SEMINAR?trainingregistry-March-2018-SEO
  • 147 Request Info

    Supplier Management Solutions | Medical Device Manufacturers

    Supplier selection and management is one of the critical issues for medical device manufacturers. Suppliers provide materials and services to the device manufacturer, which means that they can be critical to performance and delivery of your device. Neither the FDA nor your notified body regulates your suppliers (with a few exceptions). They expect you to have an effective process to ensure your suppliers perform in the regulatory environment. How well do you understand the requirements for supplier management? Could you pass a regulatory audit or inspection without any issues? Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901480SEMINAR?trainingregistry-March-2018-SEO
  • 148 Request Info

    21 CFR Part 11 Compliance Checklist- FDA Software Validation

    This interactive two-day course explores proven techniques for reducing costs associated with implementing, using, and maintaining computer systems in regulated environments. Many companies are outsourcing IT resources and getting involved with Software as a Service (SaaS) and cloud computing. These vendors are not regulated and therefore regulated companies must ensure compliance for both infrastructure qualification and computer system validation. It is the regulated company that wants to avoid FDA form 483s and warning letters. The seminar is intended for regulated companies, software vendors, and SaaS/Cloud providers. The instructor addresses the latest computer system industry standards for data security, data transfer, audit trails, electronic records and signatures, software validation, and computer system validation. Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901525SEMINAR?trainingregistry-March-2018-SEO
  • 149 Request Info

    Medical Device Supplier Management Training | Switzerland

    This two-day hands-on course provides a clear understanding of the underlying principles of supplier management. The course uses exercises to solidify understanding. In addition, the course uses FDA Warning Letters to illustrate the points and help you learn from others. As part of the practical implementation, the course includes receiving acceptance activities, outsourced processes, process validation at the suppliers' location, supplier auditing techniques, and supplier issues in management review. Read More:
  • 150 Request Info

    Webinar on No More Excuses! Unleash the Power of Accountable Communication

    In this interactive session attendees will learn how to unleash the power of accountable communication to stop the blame game, banish excuses and boost productivity. A single, powerful factor separates super-achieving teams from those that throw around phrases like 'not my job' and 'nobody told me': Accountability. Humans are more creative, more responsive to challenges, and more capable of serving the needs of others when they are held accountable.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/No-More-Excuses-Unleash-the-Power-of-Accountable-Communication-508823/JANUARY-2018-ES-TRAININGREGISTRY
  • 151 Request Info

    Webinar on Raw Material Identification of Pharmaceuticals using QA and QC Analytical Instruments

    This program will address approaches to selecting primary and secondary suppliers of raw materials, developing an incoming receipt and testing process, adequate and appropriate storage, and other considerations for the raw materials used in drug product processing. The information obtained will also enable completion of the raw material information in Module 3 of a CTD application. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Raw-Material-Identification-of-Pharmaceuticals-using-QA-and-QC-Analytical-Instruments-503753/JANUARY-2018-ES-TRAININGREGISTRY
  • 152 Request Info

    Webinar on Intelligent Approach to Risk-Based Monitoring to Improve Clinical Trial QualityROs and sponsors serious about driving clinical trial qualit

    ROs and sponsors serious about driving clinical trial quality, efficiency, and oversight, are aware of the FDA guidance: "A Risk-Based Approach to Monitoring." From a practical level, how do you start your program and gain the full advantages of RBM? This course will provide opportunities to practice the necessary skills to apply a risk based approach to monitoring activities. This webinar will help you how to ensure that your data and supporting documentation are in the appropriate format to comply with regulatory authority inspection. Risk based monitoring can contribute to better oversight and more efficient use of resources of clinical studies. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Intelligent-Approach-to-Risk-Based-Monitoring-to-Improve-Clinical-Trial-Quality-508756/JANUARY-2018-ES-TRAININGREGISTRY
  • 153 Request Info

    Webinar on Successfully Integrating Culture during a Merger or Acquisition

    During a significant change like a merger or acquisition, listening, architecting and integrating both cultures are critical for maximizing the value of the deal. Organizations that thrive in today's complex business environment benefit from dynamic, robust cultures. It's common knowledge that mergers often fail or fall short of realizing expected value due to complications during cultural integration. When surveyed, many CEOs reported that they had no plan in place for integration and even if they did, they wished in hindsight that they'd had devoted more time and resources to cultural integration. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Successfully-Integrating-Culture-during-a-Merger-or-Acquisition-504659/JANUARY-2018-ES-TRAININGREGISTRY
  • 154 Request Info

    Webinar on NFPA 70E 2018 Standard for Electrical Safety in the Workplace: Changes From 2015 and Practical Implementation

    The NFPA 70E Standard for Electrical Safety in the Workplace has been updated for 2018. This updated standard contains significant changes when compared to the 2015 version. The course covers the requirements for working safely in the electrical environment based on the NFPA 70E. The webinar will discuss the core changes in the NFPA 70E 2018 standard and practical implementation of the changes. Special attention will be paid to the furthering of the philosophy of risk assessment and some lessons companies are learning to maintain the compliance with the standard and best practices. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/NFPA-70E-2018-Standard-for-Electrical-Safety-in-the-Workplace-Changes-From-2015-and-Practical-Implementation-507289/JANUARY-2018-ES-TRAININGREGISTRY
  • 155 Request Info

    Webinar on The Top 10 Mistakes New Managers Make and How to Avoid Them: Get the Best from Each person on your Team

    The session will give you insight of the 10 common mistakes that newly transitioned managers and essential techniques tips on how to avoid them. Unfortunately, being good at your job doesn’t guarantee that you will be a good leader or manager. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/The-Top-10-Mistakes-New-Managers-Make-and-How-to-Avoid-Them-Get-the-Best-from-Each-person-on-your-Team-503139/JANUARY-2018-ES-TRAININGREGISTRY
  • 156 Request Info

    Webinar on Improving Coaching Style for Long Term Success

    Whether you are working on developing your team or developing yourself, you will want to operate more as a coach rather than a manager. Motivating others through the role of a coach will provide you with the opportunity to have a positive impact on your entire organization. Coaching effectively and frequently can improve your business results. If you would like to know what is different about a coaching approach and how it can benefit you, your team, and your organization then this is the webinar for you. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Improving-Coaching-Style-for-Long-Term-Success-503691/JANUARY-2018-ES-TRAININGREGISTRY
  • 157 Request Info

    Webinar on Drug Product Stability and Shelf-Life

    This presentation covers the design and execution of stability studies in support of the establishment of retest dates for clinical materials and expiration dates for commercial materials. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Drug-Product-Stability-and-Shelf-Life-504782/JANUARY-2018-ES-TRAININGREGISTRY
  • 158 Request Info

    Webinar on Preparing a Proactive Root Cause Analysis with the Ishikawa Fishbone Tool

    What do you do next after you have found a non-conformance? Trying to do an uninformed 'fix' could do more harm than good, if we fix the wrong thing. All we'll do is damage the credibility of our corrective action processes and create doubts about our abilities to fix the weaknesses in our Management System. By using the Ishikawa Fishbone diagram we can take a structured approach to getting to the root of the problem. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Preparing-a-Proactive-Root-Cause-Analysis-with-the-Ishikawa-Fishbone-Tool-508166/JANUARY-2018-ES-TRAININGREGISTRY
  • 159 Request Info

    Webinar on How to Break Into Brazilian Market - A Regulatory Overview for Cosmetics and Personal Hygiene Products

    This webinar will provide an understanding of the Brazilian market regulatory rules and requirements for cosmetics and personal hygiene products. Attendees will acquire valuable information on the hottest topics allowing them to plan and enter the Brazilian market on a timely and legal manner. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/How-to-Break-Into-Brazilian-Market-A-Regulatory-Overview-for-Cosmetics-and-Personal-Hygiene-Products-508100/JANUARY-2018-ES-TRAININGREGISTRY
  • 160 Request Info

    Webinar on Biopharmaceutic Considerations in Drug Product Design and In Vitro Drug Product Performance

    This webinar will demonstrate how biopharmaceutics may be used in the rational design of a drug product to achieve a desired therapeutic objective. Furthermore, the webinar will discuss the measurement of drug product performance, in vitro, including drug dissolution and in vitro in vivo correlation. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Biopharmaceutic-Considerations-in-Drug-Product-Design-and-In-Vitro-Drug-Product-Performance-502689/JANUARY-2018-ES-TRAININGREGISTRY