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Courses

  • 21 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
  • 22 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
  • 23 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
  • 24 Request Info

    Webinar On Surviving OSHA Audit in Six Easy Steps

    Learn how to quickly spot violations in the workplace and how to correct them to OSHA standards by attending this webinar. The attendee will also be made aware of the most frequent violations, compliance strategies and the defense against citation. OSHA has a playbook that is used by each compliance and safety officer; the attendees will learn how to obtain a copy for free and tips for learning the content.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/SURVIVING-OSHA-AUDIT-502046/FEBRUARY-2017-ES-TRAININGREGISTRY
  • 25 Request Info

    Webinar On SOP for Allergen Control Plan

    This webinar will describe how to create an Allergen SOP to control all potentially hazardous allergens used in production of food. During the course of the webinar we will detail 8 major allergens, proper receipt and storage for allergens, handling of allergens, separation required for each allergen type and non-allergens, equipment needed, labeling procedure needed, allergen testing and lab resource for testing, recalls that have been necessitated due to allergens, cleaning procedures for allergens, production planning for when running allergen products.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/SOP-ALLERGEN-CONTROL-PLAN-501982/JANUARY-2017-ES-TRAININGREGISTRY
  • 26 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
  • 27 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. 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/SAFE-WORK-PRACTICES-501670/DECEMBER-2016-ES-TRAININGREGISTRY
  • 28 Request Info

    Webinar On Improving Workplace Safety with Lean Manufacturing Principles

    This webinar will provide different perspective on how to implement lean safety as part of the process to manage a small business or any industrial facility.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/WORKPLACE-SAFETY-LEAN-MANUFACTURING-501648/NOVEMBER-2016-ES-TRAININGREGISTRY
  • 29 Request Info

    Webinar On Labeling of genetically modified organisms (GMO's) in the USA

    Attend this webinar to learn an overview of the status of GMO's in the U.S., how they are regulated by the FDA, FDA's Biotechnology Policy and Biotechnology Consultation program and GMO labeling around the world. The session will refer to all FDA regulations and policies regarding GMOs as well as proposed federal, state and consumer GMO labeling initiatives.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/LABELING-GMOs-USA-501498/JUNE-2016-ES-TRAININGREGISTRY
  • 30 Request Info

    Webinar On 21 CFR 111 GMP Dietary Supplement Laboratory

    Dietary supplements are governed by 21 CFR 111 in production, testing, storage, and distribution. Although dietary supplements are not pharmaceuticals they are still subject to stringent regulations designed to insure safety and consistency of the products. This webinar will address multiple subparts of 21 CFR 111 specifically discussing laboratory facilities, equipment/instrumentation and process controls.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/21-CFR-111-GMP-DIETARY-SUPPLEMENT-LABORATORY-501499/JUNE-2016-ES-TRAININGREGISTRY
  • 31 Request Info

    Webinar On Electronic Data Integrity in a GxP Environment: Managing the Data Lifecycle for Compliance

    The FDA guidance has rapidly increased the use of electronic data capture. Pharma and Investigators seek to minimize the burden of documentation in the conduct of clinical trials. Pursuance of that goal without focus on inspectional compliance can incur a failed regulatory inspection.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/ELECTRONIC-INTEGRITY-GXP-ENVIRONMENT-501420/JUNE-2016-ES-TRAININGREGISTRY
  • 32 Request Info

    Webinar on Drafting a Software V&V Documentation Package and Protocol

    Overview: The verification and validation of medical software is coming under increased scrutiny by the U.S. FDA. This webinar will address the use of the FDA, DAMP, and other applicable industry software validation models, coupled with the ISO 14971 / ICH Q9 Risk Management models, to structure, run, and document acceptable software validations. The FDA and other regulatory agencies have stated that software validation can only be accomplished effectively if "risk-based". How can this be realistly accomplished.
  • 33 Request Info

    Conference about Sample Size and Statistical Rationale for Medical Device Packaging Validations

    Overview: Compliance to ISO 11607, Parts 1 and 2 require that Packaging Validations include the development of a statistical rationale to support the testing conclusions of sterile barrier systems and packaging processes. Learn the basics of a process for developing a validation statistical rationale for packaging sterile barrier systems and processes. Areas Covered in the Session: Statistical Rationales-the importance and application of developing an appropriate sample size for testing Compliance and guidance for: Medical device sterile barrier systems
  • 34 Request Info

    Remember Charlie Safety Training Video

    Remember Charlie is the best selling safety training video of all time. This video will captivate your employees and they will leave the training session with a new appreciation for the company safety policies and procedures.