Environmental Laws and Compliance

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  • 1 Request Info

    Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers:2-Day In-Person Seminar

    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.
  • 2 Request Info

    Combating the Prescription Opioid Crisis| Drug-Free Workplace Policies

    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
  • 3 Request Info

    Complete 1099, TIN Matching, B-Notice, FATCA and Non-resident Alien 1042-S Compliance Update 2017

    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
  • 4 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.
  • 5 Request Info

    Environmental Monitoring Investigations

    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.
  • 6 Request Info

    FDA Process Validation for Applied Statistics 2017

    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
  • 7 Request Info

    MVP Training: Environmental Laws & Compliance

    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.
  • 8 Request Info

    MVP Training: Environmental Laws & Compliance ...All States & Fed.

    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.
  • 9 Request Info

    Online Webinar on Taking the Fear out of Government Environmental Rules and Requirements

    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
  • 10 Request Info

    Quality Assurance for Microbiological Laboratories at San Francisco, CA

    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.
  • 11 Request Info

    REACH and RoHS Compliance: Gain a Deeper Understanding

    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.
  • 12 Request Info

    REACH and RoHS Compliance: Protecting Revenues with Advanced Compliance: 2-Day In-Person Seminar

    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.
  • 13 Request Info

    Root Cause Analysis and CAPA using 8-D Problem Solving Method: 2-Day Workshop

    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.
  • 14 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.
  • 15 Request Info


    TrainingToday is a leading provider of online education programs for employees & supervisors. Each course in our extensive library addresses a specific topic with engaging and interactive presentations, delivering practical advice and clear instructions.
  • 16 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
  • 17 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
  • 18 Request Info

    Webinar On An Introduction to Risks associated with Extractables, Leachables & Elemental Impurities in cGMP Manufacturing: A Project Managers Perspect

    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
  • 19 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
  • 20 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