Process Management/Mapping

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  • 21 Request Info

    Webinar On Validation and Use of Electronic Batch Records: Benefits and Implementation Planning

    This webinar discusses current topics, considerations, and controls necessary for the implementation and validation of EBR. Electronic batch record systems (EBR) are increasingly commonplace in pharmaceutical and biotechnology manufacturing environments. EBR systems are used for the automation of the execution of a batch record; they can be interfaced with many different types of systems, equipment, and instruments.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/ELECTRONIC-BATCH-RECORDS-502288/JUNE-2017-ES-TRAININGREGISTRY
  • 22 Request Info

    MRO PLANNING AND SCHEDULING TRAINING

    Click on the name of the course to be taken to our website for class schedule, class outline, and to register. Students are taught how to create a process map to help enable them to identify problems with a particular MRO line. The class then takes an extensive look at forecasting to provide students with an understanding of industry recommended procedures for reliable forecasting. Next, we examine best practices in sales and operations planning and planning and scheduling in an MRO environment. We now discuss best practices in materials resource planning (MRP), capacity management, and production activity control to learn how to make the most of what we have to work with. The class moves on to training in lean manufacturing, just in time (JIT), and the theory of constraints. The class finishes with a discussion of the latest MRO planning software and technologies. Cost of this course is $1,999.00
  • 23 Request Info

    Webinar On Get the Record Straight: OSHA's New Injury Recordkeeping E-Submission Rule

    Attending this webinar by expert speaker Joe Keenan will give you a clear understanding of your responsibility for the new electronic submittal process and ramifications to the employer.The U.S. Occupational Safety and Health Administration (OSHA) has changed elements of the 29 Code of Federal Regulation (CFR) 1904 to include electronic submittal of injury and illness data. OSHA believes this is a behavioral economic move to provide a "nudge" to employer to focus on safety. The information for injury and illness will be available publicly and is believed to help accuracy of recordkeeping data.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/OSHAs-RECORDKEEPING-E-SUBMISSION-RULE-509804/MAY-2017-ES-TRAININGREGISTRY
  • 24 Request Info

    Webinar On Solving Statistical Mysteries - What Does the FDA Want?

    This webinar provides an overview of what it appears the FDA is looking for in the use statistics by taking illustrative examples from warning letters and industry experiences and approaches that have worked in a variety of situations.Use of statistics has been part of the FDA's guidance and regulations for many years. Use of statistical tools is an integral part of the Jan 2011 FDA Process Validation Guidance. It can be argued that the FDA is looking for the pharma and biotech industries to make even greater use of statistical thinking and methods. Even with this long history, the use of statistics seems to be a source of uncertainty and anxiety for many.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/SOLVING-STATISTICAL-MYSTERIES-506995/MAY-2017-ES-TRAININGREGISTRY
  • 25 Request Info

    Webinar On Writing Effective Audit Observations

    This class is designed to give you the basics for doing an operational audit. We will discuss management and audit concepts to help you understand how the process works. We will also do some exercises to further strengthen your knowledge.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-AUDIT-OBSERVATIONS-502223/MAY-2017-ES-TRAININGREGISTRY
  • 26 Request Info

    Webinar On Hypothesis Testing for Means - A Practical Approach

    One common statistical technique, especially useful in manufacturing is the hypothesis test. While it is common, it is not always well understood. In addition, some instances can involve complicated calculations. Hypothesis testing is a statistical procedure that helps determine if a set of data, typically from a sample, is compatible with a given hypothesis. This presentation focuses on hypothesis tests involving the means of a distribution, one of the most common applications.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/HYPOTHESIS-TESTING-503403/MAY-2017-ES-TRAININGREGISTRY
  • 27 Request Info

    Webinar On Process Validation for Medical Device Compliance

    The FDA finds inadequacies in process validation with Medical Device firms frequently. In fact, the fourth most frequently-cited Form 483 observation for medical device firms is for Process Validation. Find out how you can avoid these observations and emerge from your FDA audit with zero observations! Medical device validation can be confusing, but this webinar will clear many of the misconceptions related to process validation for medical device companies and helps you to bring your validation program to ship-shape.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/MEDICAL-DEVICE-COMPLIANCE-502356/MARCH-2017-ES-TRAININGREGISTRY
  • 28 Request Info

    Webinar On Auditing API Facilities

    This webinar discusses auditing of Active Pharmaceutical Ingredients (API) facilities which is an important component of GMP quality assurance programs of pharmaceutical and biopharmaceutical firms. It is important to establish auditing function as part of a quality system and maintain monitoring and assessing it over a lifecycle of a product.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/AUDITING-API-FACILITIES-505911/MARCH-2017-ES-TRAININGREGISTRY
  • 29 Request Info

    Webinar On Lean A3 Problem Solving

    A3 Problem Solving is a hands-on Lean tool that goes beyond problem solving to include clear communication, collaboration and coaching others to strive for excellence. This is a proven approach to finding effective, real solutions while also building your lean culture. This webinar is for any organization who wishes to understand A3 thinking or develop the ability to think critically, communicate well and enable collaborative approaches to problem solving and improvement.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/LEAN-A3-PROBLEM-SLOVING-502057/FEBRUARY-2017-ES-TRAININGREGISTRY
  • 30 Request Info

    Webinar On GMP Complaint Systems, Adverse Event Reporting and Product Recalls

    This training program will provide the regulatory requirements for complaint handling in the pharmaceutical industries. The course will touch on complaint sources and details will be furnished on the interrelationships regarding complaint handling and product recalls. The course will also include timeline requirements associated with adverse event reporting.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/GMP-COMPLAINT-SYSTEMS-502049/FEBRUARY-2017-ES-TRAININGREGISTRY
  • 31 Request Info

    Webinar On Conducting Effective Investigations of Out of Specification and Atypical Laboratory Results

    This training on pharmaceutical laboratory OOS investigations will explain how to recognize and address atypical or Out Of Specification results, using approaches which have been recommended by regulatory authorities, performing appropriate investigations.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/EFFECTIVE-INVESTIGATIONS-ATYPICAL-LAB-501976/DECEMBER-2016-ES-TRAININGREGISTRY
  • 32 Request Info

    Webinar On Statistical Concepts of Process Validation

    If you conduct process validation, you need to ensure that your results are valid. Beyond the regulatory requirements, statistical approaches will help you achieve the desired result - processes that produce only conforming material. This presentation provides the background you need on the statistical approach to process validation.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/STATISTICAL-CONCEPTS-PROCESS-VALIDATION-501979/DECEMBER-2016-ES-TRAININGREGISTRY
  • 33 Request Info

    Webinar On Understanding and Implementing USP 1058 - Analytical Instrument Qualification

    This webinar is designed to provide both a regulatory compliant and practical overview of equipment / instrument qualification, including requirements associated with instrumental system validation.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/webinar/USP-1058-ANALYTICAL-INSTRUMENT-501960/DECEMBER-2016-ES-TRAININGREGISTRY
  • 34 Request Info

    Webinar On Acceptance Sampling Plans for Process Validation and Production Lot Monitoring

    This webinar will cover acceptance sampling plans for process validation and production lot acceptance. Sampling plans for attribute data are the primary focus although variable acceptance sampling plans are presented as well. The binomial distribution and its use in developing Operating Characteristic (OC) curves will be discussed.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/webinar/PROCESS-VALIDATION-PRODUCTION-LOT-MONITORING-501949/JANUARY-2017-ES-TRAININGREGISTRY
  • 35 Request Info

    Webinar On Application of CMS Quality Indicator Process in Healthcare Food Service

    The Centers for Medicare & Medicaid Services (CMS), in collaboration with public and private partners, is transforming how they conduct business and operations, connect providers and empower consumers and their beneficiaries.CMS enhances its partnerships in a delivery system where providers are supported in achieving better outcomes in health and health care at lower cost for the beneficiaries and communities they serve.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/CMS-QUALITY-INDICATOR-501905/DECEMBER-2016-ES-TRAININGREGISTRY
  • 36 Request Info

    Worhshop On Design of Experiments for Process/Product Optimization

    This course is designed to help scientists and engineers plan and conduct experiments and analyze the data to develop predictive models used to optimize processes and products and solve complex problems. Design of Experiments (DOE) is an extremely efficient method to understand which variables (and interactions) affect key outcomes and allows the development of mathematical models used to optimize process and product performance.Price:$1400.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/workshop/Design-of-Experiments-for-Process-Product-Optimization-800009/NOVEMBER-2016-ES-TRAININGREGISTRY
  • 37 Request Info

    Webinar On How to Conduct an Effective Annual Product Quality Review

    This webinar will give a brief overview of the general procedure for the preparation and documentation of the Annual Product Quality Review and also focuses on the regulations and the regulatory requirements as per US and Europe. It will also discuss the comparative evaluation about similarities and differences of requirements associated with the manufacturing of the drug product in different countries.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/EFFECTIVE-ANNUAL-PRODUCT-QUALITY-REVIEW-501733/OCTOBER-2016-ES-TRAININGREGISTRY
  • 38 Request Info

    Webinar On What Sample Size Do I Need?

    The webinar will provide important considerations when selecting sample sizes for specific applications. The knowledge gained by attending the webinar will allow practitioners to consider the implications of sample size selection prior to conducting the study and ensure that the information obtained can be useful for decision making.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/WHAT-SAMPLE-SIZE-DO-I-NEED-501604/SEPTEMBER-2016-ES-TRAININGREGISTRY
  • 39 Request Info

    Webinar On Risk Based Approach for Medical Device Design Control

    This course will explain how to manage a Design Control program that will meet FDA requirements and minimize chances of your medical device being recalled. Such a program will also help to get projects completed on time and within budget. The important and confusing question of when, in a development process, Design Control begins will be answered. The difference between pre-release and post release change control will be explained.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/RISK-BASED-APPROACH-MEDICAL-DEVICE-DESIGN-501511/AUGUST-2016-ES-TRAININGREGISTRY
  • 40 Request Info

    Webinar On The Value of Analytics for Achieving Successful Manufacturing Process Transfer

    Transfer of manufacturing processes from one facility to another may be necessary during the product development lifecycle. However, changes in equipment, reagents, and infrastructure can lead to differences in product purity/impurity profiles or glycosylation. Analytical comparability between products and processes must be established to confirm safety and prevent the need for confirmatory clinical studies.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/ANALYTICS-ACHIEVING-SUCCESSFUL-MANUFACTURING-PROCESS-TRANSFER-501639/AUGUST-2016-ES-TRAININGREGISTRY