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Courses

  • 21 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 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Compliance-with-OSHA-s-Bloodborne-Pathogens-Standard-502275/APRIL-2018-ES-TRAININGREGISTRY
  • 22 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 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Navigating-the-Requirements-under-OSHA-s-Revised-Walking-Working-Surface-Rule-505304/MARCH-2018-ES-TRAININGREGISTRY
  • 23 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 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Global-Harmonization-with-New-SDS-Safety-Data-Sheet-Format-505972/MARCH-2018-ES-TRAININGREGISTRY
  • 24 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: https://www.globalcompliancepanel.com/control/globalseminars/~product_id=901462SEMINAR?trainingregistry-April-2018-SEO
  • 25 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
  • 26 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
  • 27 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
  • 28 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
  • 29 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
  • 30 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
  • 31 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
  • 32 Request Info

    Webinar On OSHA's Hazard Materials Management & Chemical Safety

    This course will describe how to evaluate chemical hazards and develop controls to protect workers and the public from the hazard. Additionally, the webinar will discuss the need for OSHA training and present techniques for developing a safety plan that addresses the use of chemicals.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/OSHAs-HAZARD-MATERIALS-MANAGEMENT-CHEMICAL-SAFETY-504927/AUGUST-2017-ES-TRAININGREGISTRY
  • 33 Request Info

    Webinar On Implementing Effective Safety Audits

    Nobody at your facility has been hurt in more than a year. Weekly inspection forms are returned with no non-compliances. Are the facility's safety plans really working that well or is it just luck? Conducting a safety audit is one of the proven ways to answer that question.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/IMPLEMENTING-EFFECTIVE-SAFETY-AUDITS-507553/AUGUST-2017-ES-TRAININGREGISTRY
  • 34 Request Info

    Complaints, Adverse Event Reporting, and Recalls - An Integrated Approach 2017

    Medical Device manufacturers operate in numerous regulatory systems that often have different requirements and are not always consistent. The new ISO 13485:2016 emphasizes this problem. Manufacturers must identify their roles, identify the regulatory requirements for that role, and incorporate them into the quality management system. The various jurisdictions, however, deal with post-market device issues in many different ways. The quality management system, QMS, needs three interlocking process: complaint management, adverse event reporting, and recalls. These processes also have supporting QMS processes such as corrective action and design changes. Overarching the QMS processes are the regulatory requirements, usually involving record keeping and reporting. This workshop covers these primary and secondary QMS processes and analyzes them in terms of US, EU, and Canadian regulations.
  • 35 Request Info

    Validation, Verification and Transfer of Analytical Methods from FDA/EMA, USP and ICH 2017

    Analytical methods and procedures should be validated to ensure reliability, consistency and accuracy of analytical data. Compendial methods should be verified to demonstrate the suitability of laboratories to successfully run the method and when methods are transferred between laboratories successful transfer should be demonstrated through testing. In case a laboratory wants to use an alternative method instead of a compendial method, equivalency of the alternative method to the compendial method should be demonstrated. Method validation recently got highest attention from regulatory agencies and industry task forces. For example, FDA and EMA released guidelines on method validation and transfer, and USP has proposed new approaches chapters for integrated validation, verification and transfer of analytical procedures, for equivalency testing and for statistical evaluation.
  • 36 Request Info

    HIPAA - Understanding Compliance Program Requirements 2017

    Being in compliance with HIPAA involves not only ensuring that you provide the appropriate patient rights and controls on your uses and disclosures of Protected Health Information; but that you also have the proper policies and procedures in place. If audited or the subject of a compliance review, 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. If your healthcare practice, business, or organization needs to understand how to put a HIPAA compliance program in place or make sure the current program is adequate and can withstand government scrutiny, please join us for this informative and interactive two-day training course.
  • 37 Request Info

    Japan - Regulatory Filing Requirements and Compliance Processes for Medical Devices 2017

    Japan's classification system differs from that of the United States or European Union Medical devices are classified to Class I, II, III, or IV depending on their risk level Medical devices must also comply with Japanese Industrial Standards and these standards define industry-wide safety and performance requirements Strict new package insert requirements Change to MAH Licensing rules A new MAH License category for In Vitro Diagnostic (IVD) devices A new registration system for manufacturers A new QMS conformity assessment system New formats for pre-market certification and pre-market approval applications Expanded scope of third party certifications Rules for software as a medical device Rules for transferring pre-market certifications And Much More...
  • 38 Request Info

    Regulatory Filing Requirements and Compliance Processes for Medical Devices 2017

    Japan's classification system differs from that of the United States or European Union Medical devices are classified to Class I, II, III, or IV depending on their risk level Medical devices must also comply with Japanese Industrial Standards and these standards define industry-wide safety and performance requirements Strict new package insert requirements Change to MAH Licensing rules A new MAH License category for In Vitro Diagnostic (IVD) devices A new registration system for manufacturers A new QMS conformity assessment system
  • 39 Request Info

    Webinar On Risk Management in Clinical Trials: What will inspectors look for?

    Risk management is becoming increasingly important to running clinical trials. There are now numerous pharmaceutical guidelines covering risk management including ICH Q9, the revised ICH GCP guideline, recently released EU Clinical Trial Regulation guideline on risk management and several other risk management clinical research standards and initiatives.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/RISK-MANAGEMENT-CLINICAL-TRIALS-506955/AUGUST-2017-ES-TRAININGREGISTRY
  • 40 Request Info

    Webinar On Leading Indicators & Trends to Predict Health Injuries and Environmental Incidents

    Leading indicators have been used for years to predict the future. Weather professionals to predict the weather use barometric pressure. Polls are used to inform politicians if they should change their strategy and elevated body temperature or blood pressure are leading indicators concerning an individual's health.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/LEADING-INDICATORS-PREDICT-HEALTH-INJURIES-503618/AUGUST-2017-ES-TRAININGREGISTRY