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  • 81 Request Info

    eCTD Submissions of IND/NDA to the US FDA, EU and Canada

    The international agreement to assemble all Quality, Safety and Efficacy information for a drug or biologic product into a common format (called the CTD - Common Technical Document) has improved the speed and efficiency for companies working in global development programs and clarified expectations by regulatory bodies. Reformatting for multiple submissions is substantially limited. The CTD has improved the regulatory review processes and enabled implementation of good review practices. The eCTD has increased efficiency for reviewers and improved submission times. Beginning in May 2017, the eCTD will be required in the US for all marketing applications. Click to Continue Reading: https://www.globalcompliancepanel.com/control/globalseminars/~product_id=901660SEMINAR?trainingregistry-April-2018-SEO
  • 82 Request Info

    Webinar on How to Structure and Write an Occupational Safety & Health Plan

    This webinar will describe the elements and characteristics necessary for the development and writing of an occupational health and safety Plan. The main component of this Plan will be your 'Company Safety Manual' however, the actual Plan will encompass far more than a Manual.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-Structure-and-Write-an-Occupational-Safety-Health-Plan-506155/FEBRUARY-2018-ES-TRAININGREGISTRY
  • 83 Request Info

    Webinar on EPA's New Final Rule on Hazardous Waste Generator Improvements and Biennial Reporting - Be Ready for the March 2018 Deadline!

    This final rule revises and updates the hazardous waste generator regulations. This rule is designed to make regulations easier to understand and to provide greater flexibility and explains how hazardous waste is managed in order to fit today's business activities. The revisions are also designed to protect the public by improving facility safety as it relates to hazardous waste generation and management. Further the rule improves the capabilities of the emergency responders by improving risk communication. 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/EPA-s-New-Final-Rule-on-Hazardous-Waste-Generator-Improvements-and-Biennial-Reporting-Be-Ready-for-the-March-2018-Deadline-508768/FEBRUARY-2018-ES-TRAININGREGISTRY
  • 84 Request Info

    Webinar on Developing a Risk-Management Matrix for Non-Bank Financial Institutions (NBFIs) to Comply with AML Laws

    This one-hour presentation will examine approaches and strategies for non-bank financial institutions to take in creating an effective and viable risk management system.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/Developing-a-Risk-Management-Matrix-for-Non-Bank-Financial-Institutions-NBFIs-to-Comply-with-AML-Laws-507934/JANUARY-2018-ES-TRAININGREGISTRY
  • 85 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
  • 86 Request Info

    Webinar on Identifying Cybercrimes

    Each year cyber crimes as we know are evolving. In what is a trying time for organizations, the severity of internal and external threats are mounting. While the financial repercussions of such incidents are often substantial regulatory bodies have also become more heavy-handed in penalizing organizations that fail to safeguard customer data. Join this helpful webinar to understand and identify the most current insider and external cyber-security threats. 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/Identifying-Cybercrimes-504203/JANUARY-2018-ES-TRAININGREGISTRY
  • 87 Request Info

    Webinar on How to Conduct a Mock OSHA Audit

    This training program will help attendees to learn the efficient and time-tested way to conduct an OSHA audit of their facility and then what to do with it! Attendees will also learn the OSHA hazards and how to avoid those hazards. 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-Conduct-a-Mock-OSHA-Audit-508599/JANUARY-2018-ES-TRAININGREGISTRY
  • 88 Request Info

    Preparing for the FDA's Menu Labeling Regulations and Implementation Best Practices

    Recently Foyles restaurant in Glasbury-on-Wye has been fined £7,430 by Powys County Council for falsely describing the food offered on the restaurant's menus, website and social media. With the enforcement date fast approaching of May 2018, many such lawsuits are bound to happen. Restaurant chains, grocery store delis have until May 7, 2018 to put calorie counts on their menus. 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-for-the-FDA-s-Menu-Labeling-Regulations-and-Implementation-Best-Practices-502553/DECEMBER-2017-ES-TRAININGREGISTRY
  • 89 Request Info

    OSHA Fatal Four - Why Compliance with 'Regulations' Will Not Prevent a Workplace Fatality

    OSHA and the Bureau of Labor Statistics have recently published data on the rate of fatalities in the category known as the 'Focus Four', also referred to as the 'Fatal Four'. The Focus Four are: Fall protection, Electrocution, Struck-by and caught-in or -between. Anyone in the safety business will readily attest to the lethality of these categories. What the statistics have shown is that over the past five years, falls and electrocutions are being effectively controlled with the application of intensive training, personal protective equipment (PPE), improved protective measures, etc. 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/OSHA-Fatal-Four-Why-Compliance-with-Regulations-Will-Not-Prevent-a-Workplace-Fatality-502510/DECEMBER-2017-ES-TRAININGREGISTRY
  • 90 Request Info

    Webinar on How to Consult to Physicians and Healthcare Leaders on Compliance Issues

    This presentation is designed to provide strategies and insights for effectively consulting to physicians and healthcare leaders on compliance issues. It will cover how to think and act like a consultant, deploying a consistent process for consulting, and strategies for communicating with disengaged physicians and leaders. Using a case scenario, this presentation will walk through the steps to consult internally on a hypothetical issue and offer insights for how to approach each step in the consulting process. 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-CONSULT-TO-PHYSICIANS-AND-HEALTHCARE-LEADERS-ON-COMPLIANCE-ISSUES-502331/NOVEMBER-2017-ES-TRAININGREGISTRY
  • 91 Request Info

    Medical Device Software Risk Management Standard | Software Expert 2018

    Engineers are dedicated to making things work, so a focus on how they might fail and harm someone can seem alien. Managing risk, however, is essential for all medical products- medical devices, including those involving software, have produced some painful examples of poor risk management with serious consequences. Experience has shown that there is a better way, that it is possible to manage risk in a changing business and technical world. Regulatory bodies are placing increased emphasis on risk management, and technology shifts are introducing new sources of risk. Newer Lean-Agile methods are recognized by the FDA as a good way to accomplish risk management. Techniques for risk management are well established, but require specific interpretation when applied to software. keep enhancing: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901345SEMINAR?trainingregistry-January-2018-SEO
  • 92 Request Info

    Pharmaceutical Validation Guidelines | 21 CFR Part 11 Compliance 2018

    Computer Systems Validation (CSV) also known as Software Validation is all-pervasive in the Life Sciences Industry. It is a requirement of all the predicate rules, as well as 21 CFR 11 and Annex 11. However, unless one knows how to implement CSV, it is often very hard to detect the requirement for CSV, and very hard to determine what needs to be done, to meet domestic and / or international regulations or business continuity requirements. In addition, the FDA has stepped up 21 CFR 11 inspections that include CSV. This course will build on the Validation and 21 CFR 11 Compliance Basic Course, to give hands on experience on executing on the computer systems validation of a system, and to discuss related activities such as Validation Master Plan, Infrastructure Qualification, Project Management for Validation and Validation of Test Tools keep enhancing: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901444SEMINAR?trainingregistry-January-2018-SEO
  • 93 Request Info

    Webinar on Prepaid Account Regulations: A Readiness Checklist

    This payments webinar will review the products covered by the regulation and the criteria used to determine coverage. Also very important to understand is the information that must be disclosed to the consumer at the time of purchase whether in a store, branch office, online or via phone and finally we will discuss Regulation E protection requirements. Our prepaid card webinar will conclude with the transaction history requirements and provide a deep-dive into the requirements for over-draft coverage and the conditions under which Regulation Z requirements must be followed. The payments webinar will finish with implementation of effective date requirements. 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/PREPAID-ACCOUNT-REGULATIONS-A-READINESS-CHECKLIST-509967/NOVEMBER-2017-ES-TRAININGREGISTRY
  • 94 Request Info

    Webinar on How to Develop Clear, Concise, and OSHA-Compliant Procedures and Instructions

    Developing and implementing clear and concise safety procedures is the best way to ensure that employees safely perform their assigned tasks, reduce workplace injuries and illnesses, and meet OSHA regulatory requirements. This webinar will cover the basics of how to take potentially cumbersome written OSHA compliance policies and turn them into an employee user-friendly format. This will help with employee buy-in and engagement with safety and help to ensure OSHA compliance is maintained. Creating Job Safety Analysis/Job Hazard Analysis (JSA/JHA) can help supplement complicated OSHA written safety procedures. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://onlinecompliancepanel.com/webinar/HOW-TO-DEVELOP-CLEAR-CONCISE-AND-OSHA-503337/NOVEMBER-2017-ES-TRAININGREGISTRY
  • 95 Request Info

    FDA's Latest Regulations for Computer Systems Used in the Tobacco and Related Industries, Effective 08/08/2016

    The Tobacco Control Act went into effect by FDA on June 22, 2009. Through this ruling, the FDA regulated cigarettes, cigarette tobacco, roll-your-own tobacco and smokeless tobacco, but in 2016, the FDA finalized a rule, Deeming Tobacco Products To Be Subject to the Federal Food, Drug, and Cosmetic Act, which extends the FDA's authority to include the regulation of electronic nicotine delivery systems (such as e-cigarettes and vape pens), all cigars, hookah (water pipe) tobacco, pipe tobacco and nicotine gels, among others. The rule went into effect on August 8, 2016. This action is a milestone in consumer protection. Going forward, the FDA Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901294SEMINAR?trainingregistry-December-2017-SEO
  • 96 Request Info

    Applied Statistics for Scientists and Engineers 2017

    Throughout 21 CFR and guidance documents for the pharmaceutical, biopharmaceutical, and medical device industries, the application of statistical methods are specified for: setting validation criteria and specifications, performing measurement systems analysis (MSA), conducting stability analysis, using design of experiment (DOE) for process development and validation, developing process control charts, and determining process capability indices. Different statistical methods are required for each of these particular applications. Data and tolerance intervals are common tools used for setting acceptance criteria and specifications. Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901138SEMINAR?trainingregistry-December-2017-SEO
  • 97 Request Info

    Why you Should be Worried about HIPAA 2017

    This seminar will be addressing how practice/business managers (or compliance offers) need to get their HIPAA house in order before the imminent audits or (even worse) litigation occurs against your organization under state laws of negligence. It will also address major changes under the Omnibus Rule and any other applicable updates for 2017. Areas covered will be texting, email, encryption, medical messaging, voice data and risk factors as they relate to IT. The primary goal is to ensure everyone is well educated on what is myth and what is reality with this law, there is so much misleading information all over regarding the do's and don'ts with HIPAA - I want to add clarity for compliance officers Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901048SEMINAR?trainingregistry-December-2017-SEO
  • 98 Request Info

    Quality by Design using Design of Experiments (QbD) 2017

    This seminar focuses on how to establish a systematic approach to pharmaceutical development that is defined by Quality-by-Design (QbD) principles using design of experiments (DOE). In addition, this course teaches the application of statistics for setting specifications, assessing measurement systems (assays), developing a control plan as part of a risk management strategy, and ensuring process control/capability. All concepts are taught within the product quality system framework defined by requirements in regulatory guidance documents. Using a QbD approach for pharmaceutical development studies should include a systematic understanding of the process and using this understanding to establish a control strategy as part of a comprehensive quality risk management program. Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901134SEMINAR?trainingregistry-December-2017-SEO
  • 99 Request Info

    Auditing Analytical Laboratories for FDA Compliance 2017

    Auditing analytical laboratories can be complex because of the preparation that is often required. All of the GMP rules do not apply to the laboratory; while there may be additional requirements depending upon the type of testing that is being conducted. In many cases, the laboratory itself may not understand what regulations apply to the work that is being conducted. Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901324SEMINAR?trainingregistry-November-2017-SEO
  • 100 Request Info

    Implementing ISO 13485:2016- 2017

    The final version of ISO 13485:2016 is now available and companies should be planning their implementation. There are significant changes from the earlier version; they will require major modifications to the Quality Management System (QMS). The new version has better alignment with FDA's QSR, but there are still major differences that create issues for effective QMS implementation. Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901112SEMINAR?trainingregistry-November-2017-SEO