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  • 1 Request Info

    Webinar on Cal/OSHA Update for 2018: Hot Spots & Practical Compliance Strategies Every Safety Pro Should Know

    Gain insight on recent and upcoming Cal OSHA regulatory developments and trends that will impact California employers in 2018-which is right around the corner. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 2 Request Info

    Webinar on Understand New 20 CFR 1926 Subpart AA - Confined Spaces in Construction

    Learn in detail about OSHA's final rule regarding confined spaces for construction and General Industry. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 3 Request Info

    Webinar on Compliance with OSHA's Bloodborne Pathogens Standard

    The presenter Edgar Fernandez describe and explain the steps required to establish a Bloodborne pathogen program that is in compliance with OSHA's requirements. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 4 Request Info

    Webinar on Navigating the Requirements under OSHA's Revised Walking-Working Surface Rule

    What are the new requirements for managing slip, trip and fall hazards in general industry and the criteria for fall protection equipment and ladder safety Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 5 Request Info

    Webinar on Global Harmonization with New SDS (Safety Data Sheet) Format

    OSHA has made a significant revision to the HazCom Standard with the new Globally Harmonized Standard (GHS) with a new Safety Data Sheet (SDS) format. This webinar will give participants a comprehensive overview of the new OSHA GHS requirements. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 6 Request Info

    Webinar on Creation of an EHS Compliance, Technical or Management System Audit Protocol

    Learn the importance of EHS auditing. The results of an audit should not be a surprise they should be confirmatory. By attending this webinar you will learn how an audit can and should be non-adversarial. You will learn what to do should a significant noncompliance situation be identified during a compliance audit. Remember it is far better to conduct an internal audit, or have an audit conducted by a hired consultant and learn of noncompliant situations than it is to learn of them as a result of a regulatory agency inspection.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 7 Request Info

    Webinar on Accident Causation and Investigation

    In the accident causation and investigation, the team will conduct a detailed procedure for discovering the root cause of the accident. The root cause goes beyond "operator error" and "equipment failure". All incidents, including near misses, must be reported and investigated to prevent injuries, illnesses, and fatalities in the workplace. However, not all employers have developed the skills needed to conduct an effective accident investigation. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 8 Request Info

    The Use of Drug Master Files & Quality Agreements: Understanding and Meeting your Regulatory and Processing Responsibilities

    This combined DMF (Drug Master Files) and Quality Agreement training will discuss the advantages for suppliers and drug product manufacturers in developing these arrangements together. Over time, there have been several misunderstandings between supplier / contractors and pharmaceutical / biologic finished product manufacturers. The root of many of the problems lie in a lack of a suitable agreement delineating roles, responsibilities and resolution to agreement to these issues. Part of these arrangements typically involve the development, support and updating of confidential technical files (Drug Master files), which allow suppliers to protect their confidential product and process information from each and every customer and share it only with the Agency. Click to Continue Reading:
  • 9 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:
  • 10 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 Event link
  • 11 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 Event link
  • 12 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 Event link
  • 13 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 Event link
  • 14 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 Event link
  • 15 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 Event link
  • 16 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:
  • 17 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:
  • 18 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 Event link
  • 19 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 Event link
  • 20 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: