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Courses

  • 1 Request Info

    Webinar On EPA's Final Rule on Hazardous Waste Generator Improvements

    You should attend this webinar if your facility is in any way connected with the generation, treatment, storage, disposal or transport of hazardous waste. If your facility generates hazardous waste you should be familiar with the existing rule and what it takes to maintain compliance. This webinar will present information on the changes to the rule; and how your facility will be affected.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/EPAs-FINAL-RULE-HAZARDOUS-WASTE-GENERATOR-502037/FEBRUARY-2017-ES-TRAININGREGISTRY
  • 2 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
  • 3 Request Info

    Seminar on Requirements for Establishing an Effective Cleaning Validation Program

    Overview: This 2 day course will cover practical guidance on cleaning validation regulatory compliance, in conjunction with, risk-based, reasonable and informed decision making and activity planning. This two day interactive course will cover fundamental principles of a cleaning validation program, exploring such concepts as the determination of residues to be targeted, selection of analytical and sampling methods, determination of appropriate limits in various pharmaceutical and biotechnology processes, and establishment of scientific rationales acceptable to regulatory inspectors.
  • 4 Request Info

    Webinar On AML Model Validation: A Critical Need in the New Regulatory Environment

    This training program will discuss the history and origin of a model validation. It will also discuss the requirements by the OCC for a model validation, and what exactly a model validation should include. The session will also cover the elements of a model validation in-depth to know what to look for in an RFP.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/AML-MODEL-VALIDATION-501840/NOVEMBER-2016-ES-TRAININGREGISTRY
  • 5 Request Info

    Webinar On Transition to the Revised Total Coliform Rule (RTCR) - Public Water System Training

    The Environmental Protection Agency (EPA) published the Revised Total Coliform Rule (RTCR) in the Federal Register (FR) on February 13, 2013 (78 FR 10269) and minor corrections on February 26, 2014 (79 FR 10665). The RTCR is the revision to the 1989 Total Coliform Rule (TCR) and is intended to improve public health protection.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/REVISED-TOTAL-COLIFORM-RULE-501831/OCTOBER-2016-ES-TRAININGREGISTRY
  • 6 Request Info

    Preparing Effective Environmental Compliance and Safety Management Plans and Manuals

    This webinar will instruct you on how to develop plans and manuals that will meet the needs of your employees, insurance companies, facilities that you do work for, and regulators. Who Will Benefit: Business Owners Construction Executives Environmental Supervisors Safety Managers & Directors Legal Counsel Project Managers Project Sponsors Project Control Personnel Safety Professionals Instructor Profile: Keith Warwick, PE earned a B.S. in civil engineering from the University of California at Davis. He became a California Professional Engineer in 1983 and has also held PEs in Indiana, Tennessee, Illinois and New York. He has 34 years of civil, environmental and safety engineering experience. He is a professor at Yuba College in Marysville California and has experience teaching engineering, safety and related subjects. Note: Use coupon code NB5SQH8N and get 10% off on registration.
  • 7 Request Info

    Webinar On Production and Process Control: Building a Robust System for Medical Device Companies

    Production and Process Controls (P&PC;) are one of the key capabilities necessary for medical device companies to consistently and effectively produce products. P&PC; is critical to producing safe and effective products for your customers. It is a broad area covering environmental, personnel, contamination, building, equipment, inspection, materials, and more. Because of its criticality, P&PC; is one of areas most closely inspected by the FDA. This webinar will help you understand what is necessary for P&PC; and how to integrate it seamlessly with the rest of your Quality Management System.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/PRODUCTION-PROCESS-CONTROL-MEDICAL-DEVICE-501676/OCTOBER-2016-ES-TRAININGREGISTRY
  • 8 Request Info

    Webinar On Handling, Storage, Distribution, and Installation of Medical Devices

    Handling, storage, distribution, and installation are often forgotten and neglected parts of the Quality Management System (QMS) for medical device companies. But, failure to fully establish these processes in your company can still have a serious impact on your company and on your customers. Failures can negatively impact your business in terms of manufacturing efficiencies, your inventory levels, scrap, yields, and more.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/HANDLING-STORAGE-DISTRIBUTION-INSTALLATION-MEDICAL-DEVICES-501674/SEPTEMBER-2016-ES-TRAININGREGISTRY
  • 9 Request Info

    Webinar On EHS Incident Prevention - Proactive EHS Programs

    This training program will offer participants an understanding of the importance of recognition of hazards, and potentially unsafe conditions before serious EHS incidents and events occur. The course will focus on EHS incident prevention and creating proactive EHS programs.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/EHS-INCIDENT-PREVENTION-501557/AUGUST-2016-ES-TRAININGREGISTRY
  • 10 Request Info

    Conference about Basic Cleaning with Environmental Cleaning

    Companies must provide effective Food Safety training for all employees including managers, supervisors, sanitation employees and production employees in order to produce a safe quality food product. The Understanding of basic cleaning principles and the chemistry of cleaning enhances a food plants overall sanitation program. Proper Environmental Cleaning is just as important as the cleaning of the "inside" of food processing equipment. The exterior of equipment, floors, walls, ceilings, doorways and drains can be a major source of microbial contamination if not properly controlled.
  • 11 Request Info

    Webinar On Are You Ready For The FDA's Mandate Requiring Electronic Submission Conformance to SEND and SDTM?

    In this course, we will examine the 'why' behind the mandate and how it can change the way therapies are being developed, leading to faster market delivery of better drugs. We will explore FDA's vision of having electronic access to all submission data in ways that are not currently feasible. The electronic standards for exchange of nonclinical data (SEND) and clinical data (SDTM), developed by CDISC, will be discussed, focusing on SEND.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/FDAs-MANDATE-REQUIRING-ELECTRONIC-SUBMISSION-SEND-SDTM-501623/AUGUST-2016-ES-TRAININGREGISTRY
  • 12 Request Info

    Webinar On TSCA Reform - What's Next?

    Attendees will gain knowledge of recent policy changes related to Toxic Substances Control Act (TSCA) and the potential impacts on their business. The program will provide insight on how to stay ahead of policy changes and prepare for new regulatory responsibilities. Attendees will get tips on how to engage with policy officials to provide input on the regulatory implementation of policy changes.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/TSCA-REFORM-WHATS-NEXT-501612/JULY-2016-ES-TRAININGREGISTRY
  • 13 Request Info

    Webinar On Writing Effective Environmental Impact Statements (EIS) Under National Environmental Policy Act (NEPA)

    Learn How to Write Winning Environmental Impact Statements (EIS) with the Public in Mind. If you're planning or consulting on a project that requires federal or state action - and you want to see it finished - you must know about National Environmental Policy Act (NEPA) and its state equivalents.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/WRITING-EFFECTIVE-EIS-NEPA-501503/JUNE-2016-ES-TRAININGREGISTRY
  • 14 Request Info

    Webianr On Writing Effective Email

    Have you been on the receiving end of an email with an endless, useless recipient list? Have you struggled through the overlong, cryptic prose and twisted logic of an email only to realize you have received a message whose business does not concern you? Have you suffered bizarre or puzzling formatting, emoticons, and smileys? Problems in email communication have led to executives overwhelmingly concluding that staff email is used inappropriately-either as a weapon for assaulting readers from a safe distance or as an excuse to avoid communicating in person.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/WRITING-EFFECTIVE-EMAIL-501446/JUNE-2016-ES-TRAININGREGISTRY
  • 15 Request Info

    Webinar On Cyber Security Governance: Integration of ISO 2000-1 ITSM & ISO 27001 ISMS

    Learn how to fit ISO 2000-1 ITSM and ISO 27001 standards in your organizations effective risk management program. Register for this webinar Now.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/CYBER-SECURITY-GOVERNANCE-501523/JUNE-2016-ES-TRAININGREGISTRY
  • 16 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
  • 17 Request Info

    Webinar On Analytical Method Validation under Good Laboratory Practices (GLPs)

    This analytical method validation webinar will provide practical tips on how to validate an analytical method under the GLP requirements. It is recommended for laboratories that are under, or want to be under, Good Laboratory Practices (GLP) with FDA compliance training.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/GLPs-ANALYTICAL-METHOD-VALIDATION-501410/JUNE-2016-ES-TRAININGREGISTRY
  • 18 Request Info

    Environmental Management Systems (EMS)

    Historically, companies have managed their own environmental challenges in response to external pressure from government agencies, environmental interest groups, and citizens focusing mainly on regulatory compliance. Today, companies recognize the importance of sound environmental management practices that result in economic gain. The International Organization for Standardization (ISO) is a worldwide federation of national standards bodies. International standards covering environmental management are intended to provide organizations with the elements of an effective environmental management system (EMS) that can be integrated with other management requirements and help organizations achieve environmental and economic needs. The standards require that “each organization shall establish, document, implement, maintain, and continually improve an environmental management system in accordance with the requirements of the international standard and determine how it will fulfill these requ
  • 19 Request Info

    Environmental Regulations Overview

    This course provides an overview of major environmental laws and regulations and the specific standards that outline requirements to comply with them. The content in this course is designed to comply with the intent of the applicable regulatory requirements. Learner objectives are to: define the purpose of the Toxic Substances Control Act (TSCA); specify the purpose of the Resource Conservation and Recovery Act (RCRA); specify the purpose of the Comprehensive Environmental Response, Compensation, and Liability Act (CERCLA), also known as Superfund; specify the purpose of the National Environmental Policy Act (NEPA); and identify the intent of various laws. This course was developed with subject matter support provided by EnSafe Inc., a global professional services company focusing on engineering, environment, health and safety, and information technology.
  • 20 Request Info

    Hazardous Waste Generator (RCRA)

    This course provides basic information on hazardous waste determination and characterization. In addition, this course describes the three types of generator status (Conditionally Exempt Small Quantity Generator, Small Quantity Generator, and Large Quantity Generator) along with applicable requirements. Generators must manage their hazardous waste per the Resource Conservation and Recovery Act (RCRA) regulations. Thus, accumulation, labeling, and other management requirements are described for both satellite accumulation areas and 90-day accumulation areas. Lastly, the importance of, and methods for, waste minimization and spill prevention and response are defined. The content in this course is designed to comply with the intent of the applicable regulatory requirements. Learner objectives for this course are to identify and characterize all wastes, properly label and manage waste containers, use a manifest when RCRA waste is transported, properly dispose of hazardous waste, prepare wa