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Courses

  • 1 Request Info

    Webinar on The Hatto ("Sudden Awareness") Report - Use Stakeholder-Initiated CAPA to Drive Improvement

    This webinar will present use of Hatto (sudden awareness) report, stakeholder-initiated CAPA to drive improvement. Price:$150.00. 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-Hatto-Sudden-Awareness-Report-Use-Stakeholder-Initiated-CAPA-to-Drive-Improvement-507502/FEBRUARY-2019-ES-TRAININGREGISTRY
  • 2 Request Info

    Webinar on Identification and Quantitation of Low-Level Compounds for Impurity and Degradation Analyses

    Understand how to have a structured approach to minor component identification and quantitation of low-level compounds for impurity and degradation. Price:$150.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link - https://www.onlinecompliancepanel.com/webinar/Identification-and-Quantitation-of-Low-Level-Compounds-for-Impurity-and-Degradation-Analyses-502236/FEBRUARY-2019-ES-TRAININGREGISTRY
  • 3 Request Info

    Webinar on Risk Based Computer System Validation

    Join this one hour webinar to learn how to integrate risk based software supplier evaluation into the computer system validation process. Price:$150.00. 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-Based-Computer-System-Validation-504574/FEBRUARY-2019-ES-TRAININGREGISTRY
  • 4 Request Info

    Webinar on Laboratory Inspection Readiness - Implementing GMPs for the Pharmaceutical Laboratory

    What are the strategies to be implemented before your laboratory undergoes a GMP inspection. Join the webinar to learn more. Price:$150.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link - https://www.onlinecompliancepanel.com/webinar/Laboratory-Inspection-Readiness-Implementing-GMPs-for-the-Pharmaceutical-Laboratory-504036/JANUARY-2019-ES-TRAININGREGISTRY
  • 5 Request Info

    Webinar on OSHA's Voluntary Protection Program

    Learn the best practices in implementing the OSHA VPP program. Register for this one hour webinar by Keith Warwick. Price:$150.00. 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-s-Voluntary-Protection-Program-504803/JANUARY-2019-ES-TRAININGREGISTRY
  • 6 Request Info

    Webinar on GMP's for Medical Marijuana - Insight into Manufacturing, Labeling, Tracking and Disposal requirements

    Know the basics of GMPs for any medical marijuana production operation, so that your unit is fully compliant when cannabis is federally recognized. Live Webinar. Price:$150.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link - https://www.onlinecompliancepanel.com/webinar/GMP-s-for-Medical-Marijuana-Insight-into-Manufacturing-Labeling-Tracking-and-Disposal-requirements-505324/JANUARY-2019-ES-TRAININGREGISTRY
  • 7 Request Info

    Why Humans Error and What We can do About it

    Every system has a goal. Some systems may have more than one. The purpose of each part of a system is to successfully execute its task or tasks in order to support achieving that system goal or goals. Management of the design and operation of a system is to mitigate against failure of each part of a system in order to ensure the system goal is achieved.
  • 8 Request Info

    Webinar on New Hazardous Waste Generator Rule: Your Haz Waste Compliance Obligations under the EPA's Final Generator Rule Are Now in Effect

    This webinar will evaluate an existing program to identify and address compliance challenges with the New Hazardous Waste Generator Rule. 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/New-Hazardous-Waste-Generator-Rule-Your-Haz-Waste-Compliance-Obligations-under-the-EPA-s-Final-Generator-Rule-Are-Now-in-Effect-508299/JUNE-2018-ES-TRAININGREGISTRY
  • 9 Request Info

    Webinar on Silica Dust Exposure Avoidance and How to Comply With the Revised OSHA Standard

    Join this webinar to discuss the applied control techniques for achieving compliance with the newly revised OSHA silica dust exposure standard. 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/Silica-Dust-Exposure-Avoidance-and-How-to-Comply-With-the-Revised-OSHA-Standard-506534/MAY-2018-ES-TRAININGREGISTRY
  • 10 Request Info

    Webinar on Are you ready for the new ISO 45001:2018?

    Get a thorough understanding on key elements of ISO 45001 and how to migrate from an existing OSHA 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/Are-you-ready-for-the-new-ISO-45001-2018-508262/MAY-2018-ES-TRAININGREGISTRY
  • 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 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
  • 12 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
  • 13 Request Info

    Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes 2017

    Global Medical Device Regulations continue to evolve, as devices become more diverse and sophisticated. Understanding the regulations and requirements in your targeted markets will expedite speed-to-market of innovative products and assist patients needing access to life-saving products and technologies. Government Regulatory Authorities, needing to become more efficient with their time, are looking for ways to better use their internal resources without compromising safety in products, which become marketable. One such example is the Medical Device Single Audit Program [MDSAP], where Authorized Organizations would be allowed to carry out a single GMP audit on medical device manufacturing facilities and have it stand to support registrations across the current participating member countries: U.S. Canada, Brazil, Australia and Japan.
  • 14 Request Info

    Webinar On Lyophilization: What you need to Know, Validation and Regulatory Approaches

    More and more of today's (and tomorrow's) drugs are biotech drugs, complex and often highly sensitive molecules. External factors such as oxygen, sunlight, and pH values can negatively affect biotech products, leaving marketers looking for innovative ways to protect and preserve these important compounds until they can be administered to patients. The lyophilization process can protect biological activity, extend shelf life, and even increase dosing precision. In recent years, more than 30% of parenteral Food and Drug Administration (FDA) approvals were for lyophilized drugs, and estimates predict that soon more than half of all injectable drugs will require lyophilizationPrice:$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/LYOPHILIZATION-PROCESS-FDA-REGULATORY-508301/AUGUST-2017-ES-TRAININGREGISTRY
  • 15 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
  • 16 Request Info

    Webinar On Understanding Proper Aseptic Technique and Cleanroom Behavior

    This training program will discuss how, in sterile compounding, aseptic technique is contributing to the prevention of microbiological contamination. It provides sterility, safety, and efficacy to the sterile product, especially various injections for patients. In this course, cleaning, gowning and proper methods of contamination control will be reviewed along with why cleanrooms are designed the way they are.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/ASEPTIC-TECHNIQUE-CLEANROOM-BEHAVIOR-508276/JULY-2017-ES-TRAININGREGISTRY
  • 17 Request Info

    Webinar On Safe Work Practices: OSHA Compliance with Flammable and Combustible liquids

    Flammable materials are substances that can ignite easily and burn rapidly. They can be common materials that are at the most work sites in gas, liquids or solids. In addition, flammable materials may themselves represent a health hazard. This webinar will cover only the flammable and combustible liquids handling and storage. This webinar will cover OSHA and NFPA standards that govern the handling and storage of these liquids. Currently flammable and combustible liquids are used in the pharmaceutical, chemical and other industries in different part of the 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/SAFE-WORK-PRACTICES-505171/JULY-2017-ES-TRAININGREGISTRY
  • 18 Request Info

    Webinar On OSHA 29 CFR 1910.95 - Best Practices in Implementing a Successful Hearing Conservation Program

    Are you in compliance with OSHA Standard 1910.95 with Effective Hearing Conservation Programs and Noise Monitoring! Join expert speaker Joe Keenan in this live webinar to learn the sampling requirements and the best practices for protecting your employees from the dangers of noise. Also, learn what is involved in a Hearing Conservation Program and review the requirements of 29 CFR 1910.95. Get the information and guidance to properly comply with the standards and avoid OSHA citations.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/OSHA-29-CFR-1910-95-503237/JUNE-2017-ES-TRAININGREGISTRY
  • 19 Request Info

    Webinar On Revisions to the 2017 EEO-1 Survey to Collect Summary Pay Data

    This webinar will discuss about the significant changes that the Equal Employment Opportunity Commission recently made to the EEO-1 survey, its impact on businesses and what you can do now to prepare.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/ROLE-EEOC-1-PAY-DATA-506581/JUNE-2017-ES-TRAININGREGISTRY
  • 20 Request Info

    Webinar On Working with Compressed Gas: Safe Handling, Use, and Storage

    This webinar will cover the important basic aspects of safe handling and use of compressed gas cylinders. The program will focus on key elements regarding cylinder receiving, transport, storage, and safe handling in the facility and/or laboratory. Federal regulations will be covered, including regulations from DOT, OSHA, and others (NFPA). Cylinder ID requirements, determining hydrostatic test dates and proper shipping on public roads will be addressed.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/WORKING-COMPRESSED-GAS-508282/MAY-2017-ES-TRAININGREGISTRY