Environment

This course will educate you about various key elements of sterility assurance and contamination control such as Cleanroom Regulations, Classification, Sources and types of particles, Design Requirements, Validation/Qualification, Operations, Environmental Monitoring Program requirements, Excursion investigations, DataTrending, Microbiological processes/methodology, Cleanroom cleaning/disinfection.

Join this webinar that cover in detail the background of the growing problem of prescription opioid abuse in the workplace and creating a reliable drug testing program. 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/Combating-the-Opioid-Epidemic-at-Work-Using-Effective-Drug-Testing-and-Policies-502125/JULY-2018-ES-TRAININGREGISTRY

For years the IRS has struggled with the independent contractor, the non-resident alien worker, US citizens with foreign financial accounts and tax collection. They have placed the burden on businesses, non-profits and not-for-profits as well as state and local government to report information about taxable payments they make to their account holders, vendors and customers. Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901330SEMINAR?trainingregistry-November-2017-SEO

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.

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

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.

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.

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

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

MVP Seminars LLC, is a leading nationwide provider of business training seminars, consulting professionals & exceptional coaches, with quality academic backgrounds. Please call 510-558-3495.

MVP Seminars LLC, is a leading nationwide provider of business training seminars, consulting professionals & exceptional coaches, with quality academic backgrounds. Please call 510-558-3495.

MVP Seminars LLC, is a leading nationwide provider of business training seminars at affordable prices, with top-notch providers. Follow-up monitoring program no-charge! Please call 510-558-3495. Largest family run training business in USA.

The Omnibus Rule finalizes the modifications to the HIPAA Privacy Rule, Security Rule, and enforcement rules to implement many of the privacy, security, and enforcement provisions of the HITECH Act and to make other changes to the Rules, modifies the breach notification rule, and finalizes the modifications to the HIPAA Privacy Rule to strengthen privacy protections for genetic information. Generally speaking, covered entities and business associates will have until September 23, 2013, to comply with these new provisions. This 60-minute webinar gives you an excellent overview of the new rule changes. Learn what actions to take now to achieve HIPAA compliance with the new Omnibus Rule, to pass an audit or an investigation, and to avoid civil money penalties and criminal convictions.

Managing environmental activities at facilities in light of rules and requirements is a daunting task. The number of pages of legislation and regulations can be overwhelming.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/ENVIRONMENTAL-RULES-501264/FEB-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.

Overview: QMS is the catch phrase for accreditation and is the backbone of ISO/IEC Standard 17025:2005. The Quality System Manual (QSM) is the bible in a QMS environment because, much like its predecessor, Good Laboratory Practice (GLP), it contains the policies that the laboratory is expected to follow to achieve quality results. It is in fact only the "what to do" component of a QMS. What is also needed are the "how to do it" or procedures and methods and finally the controls or evidence that it was done properly.

This 2 day seminar will go into the specifics of the REACH and RoHS regulations, provide case studies and share lessons learned so your organization can benefit from the mistakes of others. We will review the latest on both directives and will draw out key developments and key dates (if applicable) with particular emphasis on requirements for US firms. Who will Benefit: Automotive, Electronics, Medical devices, Chemical, Toys, Industrial machinery Manufacturing Professionals Anyone new to RoHS and or REACH and need to understand the regulations. Anyone responsible for RoHS and REACH compliance. Note: Use coupon code NB5SQH8N and get 10% off on registration.

Who will Benefit: This seminar will provide valuable assistance to all personnel in: Automotive, Electronics, Medical devices, Chemical, Toys, Industrial machinery Manufacturing Professionals Anyone new to RoHS and or REACH and need to understand the regulations. Anyone responsible for RoHS and REACH compliance. Quality Managers, Environmental Managers, Purchasers, Buyers.

Errors are costly. To fix errors systematically, there are Reporting and Problem-Solving Technique (8-D Reporting and A-3 Reporting in connection with the PDCA-Cycle), which not only address the symptoms, but also identify the causes for quick response and fact based decision making to remedy the cause. Sustainable error prevention and complaint processing based on the 8-D Problem Solving Technique and A-3 Reporting method are used in many industries as a popular structured method to continuously improve products, but also any kind of organizational processes, as it puts focus on sustainable error prevention and complaint handling excellence. Who will Benefit: Quality Managers Quality Professionals/Consultants ISO Coordinators/Quality Management Representatives Corrective Action Coordinators/Representatives Note: Use coupon code < REFERRAL10 > and get 10% off on registration.

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.