Environment

This online training course follows OSHA requirements for fall protection training for the construction worker who might be exposed to fall hazards. This program enables the employee to recognize the hazards of falling, and trains them in the procedures to be followed to minimize these hazards. With falls from heights being the leading cause of occupational fatalities, it is not only imperative that employers train their employees; it is also mandated by law, CFR 1926.503.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-FALL-PROTECTION-SAFETY-506072/JULY-2017-ES-TRAININGREGISTRY

This webinar will present a unique perspective on risks associated with extractables, leachables & elemental impurities (ELEI) in cGMP manufacturing of pharmaceutical, biologic and medical device products. The webinar will start with a definitional review of the topic and then present the current FDA perspective on impurities of these types in product. After that introduction, the instructor will present quality and compliance considerations related to ELEI.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/EXTRACTABLES-LEACHABLES-cGMP-MANUFACTURING-507103/JULY-2017-ES-TRAININGREGISTRY

In Guidance for Industry Process Validation: General Principle and Practices, process validation is defined as, "...the collection and evaluation of data, from the process design stage through commercial production..." The guidance further delineates the 'process design stage through commercial production' into three distinct stages of the product lifecycle: Stage 1: Process Design: The commercial manufacturing process is defined during this stage based on knowledge gained through development and scale-up activities. Stage 2: Process Qualification: During this stage, the process design is evaluated to determine if the process is capable of reproducible commercial manufacturing. Stage 3: Continued Process Verification: Ongoing assurance is gained during routine production that the process remains in a state of control. The first stage of process validation is process design. The Process Validation guidance document states: "A successful validation program depends on information and

Compressed air for pharmaceutical use is considered a critical utility as many of its applications involve direct contact with the pharmaceutical product. The design, construction and monitoring of a compressed air system is essential for maintaining a quality system without contamination of the product. Proper testing of compressed air quality according to international standards is important for both validation and ongoing monitoring of the 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/PHARMACEUTICAL-COMPRESSED-AIR-502789/MAY-2017-ES-TRAININGREGISTRY

Given the ease of receiving and viewing sexually explicit materials on cell phones, computers and social media, employers as well as employees should be concerned about claims of a hostile work environment and preventing all forms of sexual harassment in the workplace. This workshop will focus on the issue of sexual harassment, sex discrimination and how to prevent it in the workplace. It will provide an overview of sexual harassment, sex discrimination, its definition and the laws that prohibit it.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/SEXUAL-HARASSMENT-DISCRIMINATION-502025/APRIL-2017-ES-TRAININGREGISTRY

The ISO 14001 standard has been updated. If you presently have the ISO 14001 standard in place at your facility this webinar is a must! The webinar will address the changes to the standard.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/THRIVING-REVISED-ISO-14001-502667/APRIL-2017-ES-TRAININGREGISTRY

The Harmonized Tariff Schedule is an international customs classification system. It was developed by the World Customs Organization, as a tool to facilitate the world trade by creating a nomenclature that assures uniformity in its application, and at the same time address domestic issues. Not only it is used to establish tariffs and duties, but also to implement measures to protect the public health, the environment, the wild and the world safety.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/HARMONIZED-SYSTEM-RULES-508887/APRIL-2017-ES-TRAININGREGISTRY

All companies involved in international trade must understand the importance of determining the correct Harmonized Tariff Schedule provision for imported and exported products. The HTS is also used to determine whether goods are subject to "other agency requirements," quotas, or free trade agreements. U.S. Customs expects companies to use reasonable care and correctly classify its imported products at the time of entry.Price:$600.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/HARMONIZED-SYSTEM-CLASSIFICATIOIN-SERIES-509908/MARCH-2017-ES-TRAININGREGISTRY

The Harmonized Tariff Schedule is an international customs classification system. It was developed by the World Customs Organization as a tool to facilitate the world trade by creating a nomenclature that assures uniformity in its application, and at the same time address domestic issues. Not only it is used to establish tariffs and duties, but also to implement measures to protect the public health, the environment, the wild and the world safety. It has been in force since 1988. It is used for 90% of the trading world.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/HARMONIZED-SYSTEM-CLASSIFICATION-509007/MARCH-2017-ES-TRAININGREGISTRY

Attendees will get an overview of environmental monitoring investigations and tools to complete an investigation. Environmental monitoring is the method by which clean rooms are known to maintain a certain level of cleanliness. The methods by which clean rooms are monitored are through viable and non-viable testing. Through this testing, a room may demonstrate that it is out of control. This seminar will provide aspects to investigate in order to determine a root cause and appropriate actions to complete the report.

Canada's first major GHS deadline is just months away. Don't wait to get started on your compliance tasks! Canada officially adopted GHS on February 11, 2015 and implemented a series of phased-in compliance deadlines - the first of which is scheduled to go into effect on June 1, 2017. This session will provide a high level overview of Canada's adoption plans.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/WHMIS-2015-GHS-WORKPLACE-504341/MARCH-2017-ES-TRAININGREGISTRY

Virtually all labels on packaged food sold in the U.S. will need to be redesigned and substantively modified following a recent update to the information required in the 'Nutrition Facts' box. Importers and domestic producers will have between two and three years to comply with the new rules. This webinar will examine the key requirements as well as timelines and strategies for compliance. This training will provide a comprehensive overview of the sweeping new changes and the impacts on the food and beverage industry. 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/FDA-UPDATED-NUTRITION-FACTS-LABEL-502322/FEBRUARY-2017-ES-TRAININGREGISTRY

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

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

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.

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

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

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.

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

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