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  • 1 Request Info

    Webinar On New Requirement for Electronic submission of Drug Master Files (DMFs): What you need to know

    In this webinar, you will learn the required contents of Module 3 as well as the appropriate formatting. Lifecycle management and updating requirements will be discussed, including appropriate change control and sponsor notifications. You will also gain an understanding of contact points with the FDA throughout the lifecycle of the DMF, including information requests and inspections.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/DRUG-MASTER-FILES-DMFs-509436/FEBRUARY-2017-ES-TRAININGREGISTRY
  • 2 Request Info

    Webinar On Consumer E-Payments - Complying with Auditor's Standards: Specific Payments Types

    This E-payments compliance training will outline and discuss electronic payments: Including electronic checks, bankcards, payment cards, ACH, EFT/POS networks, electronic bill payment, person-to-person (P2P) and account-to-account (A2A) payment systems. We will talk about risk profiles and the quality of risk management practices as required from internal and external auditors.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/CONSUMER-E-PAYMENTS-502045/FEBRUARY-2017-ES-TRAININGREGISTRY
  • 3 Request Info

    Webinar On 21 CFR Part 11 compliance for Electronic Medical Records

    This 21 CFR Part 11 training will analyze the regulations and provides concrete guidance on compliance for Electronic Medical Records.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/21-CFR-PART-11-ELECTRONIC-MEDICAL-RECORDS-502044/FEBRUARY-2017-ES-TRAININGREGISTRY
  • 4 Request Info

    Webinar On Off-Shore Business Associates & HIPAA Compliance

    The global Internet of Things and the HIPAA Privacy and Security Rules allow Protected Health Information (PHI) created by Covered Entities in the United States to be transmitted and stored outside the United States - and outside the reach of U.S. government regulators. Risks for Covered Entities, patients and Business Associates may lurk anywhere in a world where identity theft is rampant and medical identity is the Golden Egg for identity thieves.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/OFF-SHORE-BUSINESS-ASSOCIATES-HIPAA-502042/FEBRUARY-2017-ES-TRAININGREGISTRY
  • 5 Request Info

    Webinar On Importance of Usability in Medical Device Procurement

    The FDA has progressively increased requirements for human factors and usability testing before new medical devices can be approved for market release. However, successful market release does not ensure a device is easy to use or that all potential for safety-critical errors has been mitigated. Medical device purchasers must consider incorporating human factors as a standard part of the procurement process to ensure that they are choosing the safest, most usable devices for purchase.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/MEDICAL-DEVICE-PROCUREMENT-501983/DECEMBER-2016-ES-TRAININGREGISTRY
  • 6 Request Info

    Webinar On Conducting Effective Investigations of Out of Specification and Atypical Laboratory Results

    This training on pharmaceutical laboratory OOS investigations will explain how to recognize and address atypical or Out Of Specification results, using approaches which have been recommended by regulatory authorities, performing appropriate investigations.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/EFFECTIVE-INVESTIGATIONS-ATYPICAL-LAB-501976/DECEMBER-2016-ES-TRAININGREGISTRY
  • 7 Request Info

    Webinar On Powerful Presentations: Creating, Delivering and Inspiring Your Audience to Take Effective Action Every Time

    Learn how to motivate your audience to act every time. Leading others to move forward, now! takes discipline and commitment to process. There are three stages to delivering an effective presentation: Preparation, delivery and facilitating to an Action Plan. Before making a presentation, the speaker must understand and be prepared to practice the following: a passion for subject matter, detailed research, mental preparedness and rehearsal. During, there need be focus and poise. Before concluding, the effective presenter directs their audience to take action.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/POWERFUL-PRESENTATIONS-501956/DECEMBER-2016-ES-TRAININGREGISTRY
  • 8 Request Info

    Seminar on Extracting information from geochemical data

    Most specialists strongly recommend to sample every meter of the drill core or of a trench and to use multielement analysis, rather than just asking the laboratory for gold test. There are also many other types of analysis that are ignored by the industry. But even when such analyses are requested, most of the time the fed geologist is not well trained on the necessary techniques and methods to extract all the information contained in the data. This seminar will teach you what to ask and how to extract all the important information of your data.
  • 9 Request Info

    Laboratory Accreditation: Getting there is just the beginning

    Overview: Many laboratories struggle with developing and implementing a functional quality management system that not only complies with the management and technical requirements of ISO/IEC 17025:2005 but also meets their needs. Once accreditation has been achieved many laboratories have difficulty maintaining the QMS as evidenced by the number of non-conformances cited during the subsequent biannual audits. Areas Covered in the Session: Defining a Quality Management System (QMS) Management Components of a QMS Technical Components of a QMS Method Selection, Validation and Verification Ensuring analytical competency
  • 10 Request Info

    Webinar On CMC Considerations for Successful Regulatory Submission

    This webinar is intended to provide advice on the level of detail required for regulatory submissions at different program phases. Regulatory strategy across the development program will also be discussed.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/CMC-REGULATORY-SUBMISSION-501931/DECEMBER-2016-ES-TRAININGREGISTRY
  • 11 Request Info

    Webinar On Risk Management Using ISO 14971:2007 and EN ISO 14971:2012

    Risk management is essential to device design and required by other standards, such as usability engineering, biocompatibility and electrical safety. The basis is ISO 14971:2007, but many companies don't understand the standard, don't follow the process flow, and consequently don't have an effective implementation. This presentation helps you avoid the common problems and create a compliant system.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/ISO-14971-2007-501829/DECEMBER-2016-ES-TRAININGREGISTRY
  • 12 Request Info

    Webinar On 21 CFR Part 11 and Annex 11 Compliance - Specifics Needed to Eliminate 483s

    It is quite common between departments or individuals to neglect seeing the importance of 21 CFR Part 11 and Annex 11 (ERES) Compliance. Non-QA trained personnel or those that have no direct or have indirect contact with GxP systems fail to see the consequences of their actions or that of their department.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/21CFR-PART-11-ANNEX-11-COMPLIANCE-501871/NOVEMBER-2016-ES-TRAININGREGISTRY
  • 13 Request Info

    Webinar On Tax Refund Frauds: Personal and Business Identity Theft

    It's estimated that tax fraud losses in the United States will hit $21 billion in 2016. The bulk of those losses are tax refund frauds. Tax refund fraud is where criminals gain enough information about a business or individual to file taxes in that organization or person's identity. A startling number of stolen identities to commit this fraud are gained from the victim's own employer. The IRS pays the fraudulent return, and then the real entity has difficulty filing their true return.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/webinar/TAX-REFUND-FRAUDS-501785/OCTOBER-2016-ES-TRAININGREGISTRY
  • 14 Request Info

    Webinar On What to Do When the DOT Hazardous Materials Enforcement Inspector Comes Knocking

    $175,000 Per Day is the Cost of a Hazardous Material Shipping Violation-Know How to Avoid These Costly Mistakes in 60 minutes! Join this webinar to get insights into what to expect from a hazardous materials inspection and how to make the best of it. Be better prepared to minimize exposure to violations and avoid penalties that can exceed $175,000 per infraction per day.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/DOT-HAZARDOUS-ENFORCEMENT-501729/OCTOBER-2016-ES-TRAININGREGISTRY
  • 15 Request Info

    Webinar On Acceptance Activities in QSR

    Warning Letters from FDA frequently cite Acceptance Activities. In fact, it has been in the top five most frequently cited sections over the past few years. You can avoid a Warning Letter if you understand the regulations and develop processes to implement them. This presentation provides knowledge and tools to help implement an effective system that will withstand an FDA Inspection.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/webinar/ACCEPTANCE-ACTIVITIES-QSR-501690/OCTOBER-2016-ES-TRAININGREGISTRY
  • 16 Request Info

    Webinar On FDA's Two New Draft Guidance on Software and Device Changes and the 510(k)

    This course is intended to provide an overview of 2 new FDA draft guidance documents that clarify when medical device and software manufacturers must file a 510(k) (premarket notification) for changes to an existing device and/or software integrated with a device.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/FDAs-SOFTWARE-DEVICE-510k-501790/OCTOBER-2016-ES-TRAININGREGISTRY
  • 17 Request Info

    Webinar On Chemical Safety for the 21st Century Act

    This webinar addresses the recently updated 1976 Toxic Substances Control Act (TSCA). Its new name is chemical safety in the 21st Century. The updated act is titled, "Frank R. Lautenberg Chemical Safety for the 21st Century Act." The act was named in honor of Senator Lautenberg because he was an ardent proponent of modifications to TSCA during his lifetime.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/CHEMICAL-SAFETY-21st-CENTURY-ACT-501753/OCTOBER-2016-ES-TRAININGREGISTRY
  • 18 Request Info

    Webinar On Production and Process Control: Building a Robust System for Medical Device Companies

    Production and Process Controls (P&PC;) are one of the key capabilities necessary for medical device companies to consistently and effectively produce products. P&PC; is critical to producing safe and effective products for your customers. It is a broad area covering environmental, personnel, contamination, building, equipment, inspection, materials, and more. Because of its criticality, P&PC; is one of areas most closely inspected by the FDA. This webinar will help you understand what is necessary for P&PC; and how to integrate it seamlessly with the rest of your Quality Management System.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/PRODUCTION-PROCESS-CONTROL-MEDICAL-DEVICE-501676/OCTOBER-2016-ES-TRAININGREGISTRY
  • 19 Request Info

    Certified Quality Technician (CQT) Prep – Online

    Advance your career and attain the credential of ASQ Certified Quality Technician by working through this online program. This is completely self-paced per the student’s schedule. Student progress will be monitored by the course administrator on a random basis for the online option to assess student progress and provide support. An estimated time to view slides, listen to lectures, read prescribed materials in the IQC primer, and complete IQC primer blue sheet questions is 30 hours. An additional 30 hours' study of the course materials is recommended to become prepared to take the CQT exam. Total time will be dependent on the student’s background in the topics and familiarity with the Body of Knowledge. It is also recommended that the student purchase and spend time with the IQC electronic practice exams on CDROM for maximum benefit.
  • 20 Request Info

    Certified Quality Inspector (CQI) Prep – Online

    Advance your career and invest in your future by attaining the American Society for Quality’s (ASQ) Certified Quality Inspector (CQI) credential. Working through this online program will help make sure you are prepared for the ASQ exam. Quality personnel who are preparing for the ASQ Certified Quality Inspector (CQI) exam or those who want to further their professional development. Quality Auditors, Engineers, and Managers who are interested in a refresher course would benefit from this course. The student will receive a username and password to access the online course that contains all the lectures (flash player required), special links to additional references, study materials and full email support from the author/instructor. The student MUST purchase the Quality Council of Indiana (QCI) CQI Primer to use in conjunction with the online course.