Manufacturing - Production Scheduling and Control

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  • 1 Request Info

    PRODUCTION PLANNING

    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 production 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 preparation of the master schedule. 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 finishes up with training in lean manufacturing, just in time (JIT), and the theory of constraints. Cost of this course is $1,999.00
  • 2 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
  • 3 Request Info

    Production Planning, Scheduling And Activity Control Workshop

    Learn proven techniques for planning, scheduling and controlling production activities. Develop the strategy and systems that let capacity and resources be scheduled most effectively.
  • 4 Request Info

    Webinar on Lyophilization Technology

    Overview: Lyophilization cycles consist of three phases: Freezing, primary drying, and secondary drying. Conditions in the dryer are varied through the cycle to ensure that the resulting product has the desired physical and chemical properties. Why should you Attend: The fundamental principles and technology are coupled with practical aspects of lyophilization in the training program. Principles and concepts presented are later used to discuss real world pracdtical applications. Speaker Profile: Jerry Dalfors has extensive (40 years) of business administration, consultative, technical and managerial experience in the development and manufacture of highly regulated biopharmaceutical products including injectables, biologics. Contact Detail: NetZealous - Compliance4All, 161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA. Phone: +1-800-447-9407 Email: support@compliance4All.com http://www.compliance4all.com/ Event Link : http://bit.ly/1RcUuDp
  • 5 Request Info

    FDA's 21 CFR 11 Add-On Inspections - Recent Updates

    Overview: In December 2010 FDA started the Part 11 inspection initiative. While originally the initiative was supposed to last 3-6 months, it has now turned into an ongoing program with Part 11 related issues being part of most future inspections. At the beginning of the initiative FDA made it very clear that Part 11 is in effect and is enforced according to the original Part 11 and the Guidance from 2003. In the meantime FDA officials reported about key findings. For example, George Smith who heads up FDA's Part 11 working group gave an update with examples of violations.
  • 6 Request Info

    Good Documentation Guideline (Chapter 1029 USP)

    Overview: Good Documentation Practices (GDP) is a critical and essential part of a regulated environment (pharmaceutical and medical device manufacturing, R&D, laboratories and clinical trials). Compliance with GDP ensures an auditable account of work. It ensures integrity and control of documents and is a key requirement for a developed quality system. This training session will cover the US Pharmacopeia General Chapter <1029> and all aspects of GDP including practices for writing and correcting documentation.
  • 7 Request Info

    Webinar On Comparability Protocols for Approved Drugs

    This webinar will address approaches to developing comparability protocols for approved drugs, including primary content considerations and timing of submission. The information obtained will enable completion of appropriate testing to make changes to the drug substance or drug product formulation, manufacturing facility, and container closure. The webinar will address aspects of preparing the protocol prior to confirmed changes in order to speed approval and preparing the appropriate updates to Module 3 of the CTD.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/COMPARABILITY-PROTOCOLS-APPROVED-DRUGS-501539/JUNE-2016-ES-TRAININGREGISTRY
  • 8 Request Info

    Webinar On How to Conduct a Human Factor Analysis of Instructional Documents, Particularly Master Batch Records (MBR) and Standard Operating Procedure

    This Webinar will cover how to conduct a human factors analysis of instructional documents, which is a critical task to perform for existing documents. The concepts from this session can be incorporated into the creation of new instructional documents also.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/HUMAN-FACTOR-ANALYSIS-PARTICULARLY-MBR-SOP-501574/JULY-2016-ES-TRAININGREGISTRY
  • 9 Request Info

    Webinar On Stability Studies & Estimating Shelf Life

    This webinar discusses the steps to set-up a stability study and analyze the results to estimate the product's shelf life. The use of regression models to model the relationship between the response variable(s) and time are presented. Models useful for describing non-linear degradation over time are also presented. Additionally, methods for handling non-normal response data are also discussed.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/STABILITY-STUDIES-ESTIMATING-SHELF-LIFE-501603/AUGUST-2016-ES-TRAININGREGISTRY
  • 10 Request Info

    Webinar On SMED - Single Minute Exchange of Die (reduced changeover)

    (SMED) is a methodology that was created by Shigeo Shingo in the Toyota press room to reduce the time needed to setup and changeover the huge stamping presses. The goal is first to reduce setup times by 50% and ultimately to less than 10 minutes.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/SMED-SINGLE-MINUTE-EXCHANGE-DIE-501874/NOVEMBER-2016-ES-TRAININGREGISTRY
  • 11 Request Info

    Webinar on Precisely Wrong: The Materials Planning Challenge in a Dynamic 21st Century

    What if there was one fatal flaw in MRP that makes it completely incapable of conveying relevant information? What if correcting this one fatal flaw allowed the promise of MRP to be attained? Join this webinar with expert speaker Carol Ptak, who will describe what the real issue is and just how devastating the problem can be for supply chain management. 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/Precisely-Wrong-The-Materials-Planning-Challenge-in-a-Dynamic-21st-Century-502299/JANUARY-2018-ES-TRAININGREGISTRY
  • 12 Request Info

    Webinar on Mastering Excel Pivot Tables: The Ace Analytical Tool of Excel

    A very common situation in Excel is the Big List. You might have a huge list of employees, customers, products, sales, events, locations, technical support tickets - it doesn't really matter what the list is of, what matters is that there is value in that list. You might want to know what your most profitable kind of customer is, or which technical support rep is being most productive, or which product is driving the most interest, but the Big List isn't giving you that information automatically. Building a Pivot Table is a fast, easy way of analyzing your data and giving you useful insights. If you want to know how to help your business, creating a summary and a chart with Pivot Tables should be your first move. 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/Mastering-Excel-Pivot-Tables-The-Ace-Analytical-Tool-of-Excel-506657/FEBRUARY-2018-ES-TRAIN
  • 13 Request Info

    Webinar on Stability Studies and Estimating Shelf Life with Regression Models

    Manufacturers of foods, drugs, consumer goods, and other products must determine the shelf life of their products so that customers know when the product can be expected to perform as intended. Many approaches are available to quantify the "shelf life" and the method(s) chosen often depend on the testing time available. 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/Stability-Studies-and-Estimating-Shelf-Life-with-Regression-Models-506813/MARCH-2018-ES-TRAININGREGISTRY
  • 14 Request Info

    Webinar on Process Capability: When It's Not a Bell Curve

    This process capability webinar will show how to handle situations in which the distribution is not a bell curve. 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/Process-Capability-When-It-s-Not-a-Bell-Curve-505754/APRIL-2018-ES-TRAININGREGISTRY
  • 15 Request Info

    Webinar on Sunshine Act Reporting – Clarification for Clinical Research

    This webinar will examine the implications of the Sunshine Act for healthcare providers and life science companies. 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/Sunshine-Act-Reporting-Clarification-for-Clinical-Research-508714/MAY-2018-ES-TRAININGREGISTRY
  • 16 Request Info

    Webinar on Good Documentation Practices and Recordkeeping Regulations (FDA & EMA)

    Discuss the importance of good documentation practices/GDP and how to create lab notebook policies that meet regulators expectations. 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/Good-Documentation-Practices-and-Recordkeeping-Regulations-FDA-EMA-508525/MAY-2018-ES-TRAININGREGISTRY
  • 17 Request Info

    Webinar on Processing of cGMP Controlled Raw Materials

    Join this session to discuss the implementation of risk management and knowledge management pillars for the controlled substances systems at the pharmaceutical facilities. 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/Processing-of-cGMP-Controlled-Raw-Materials-504506/JUNE-2018-ES-TRAININGREGISTRY
  • 18 Request Info

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

    Understand more about acceptance sampling plans for process validation and production lot acceptance by attending this audio conference. 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/Acceptance-Sampling-Plans-for-Process-Validation-and-Production-Lot-Monitoring-507734/JULY-2018-ES-TRAININGREGISTRY
  • 19 Request Info

    Guidance on Inactive Ingredients- FDA Update

    Attend this webinar to gain an appreciation of the regulatory CMC and use of inactive ingredients manufactured from various firms. 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/Discussion-Regarding-the-Substitution-of-a-New-Inactive-Ingredient-in-an-Approved-Parenteral-Drug-Product-505414/JULY-2018-ES-TRAININGREGISTRY
  • 20 Request Info

    Webinar on Stunning Changes in FDA's Software Regulation

    Gain an understanding of how FDA is planning to give additional regulatory relief to its regulation of software, which has a startling change for premarket access. 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/Stunning-Changes-in-FDA-s-Software-Regulation-503201/JULY-2018-ES-TRAININGREGISTRY