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Courses

  • 61 Request Info

    Manufacturing Safety - What you don't Know can Harm you

    In this webinar, we will explore the hazards related to the manufacturing facility on many fronts. To understand the plant work environment as it relates to safety, the employer must consider what the equipment the workers are exposed to on a daily basis.
  • 62 Request Info

    Expectations for Products Used in Early Phase

    FDA issued a guidance document covering GMP requirements for Phase 1 products. These guidelines remove some of the problems that are encountered with early phase products and are in addition to those that cover the CMC sections for IND submissions at Phase 1.
  • 63 Request Info

    Webinar on Supply Chain that Drives and Meets e-Commerce Customer Expectations

    Join webinar to understand what is required with supply chain management for e-commerce and satisfying customer expectations, supply chain essentials. 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/Supply-Chain-that-Drives-and-Meets-e-Commerce-Customer-Expectations-505545/APRIL-2018-ES-TRAININGREGISTRY
  • 64 Request Info

    Webinar on Tools for Success: Benchmarking for Continuous Process Improvement

    Benchmarking involves comparing your service and support organization, with a peer group. This peer group must be selected carefully. So much of what passes for benchmarking in this industry is simply a survey. Comparing the data by itself is interesting, but you need to understand how they got to a lower cost, or higher customer satisfaction, or quick mean time to respond, you can adopt and adapt what they are doing to emulate them and achieve world-class performance. 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/Tools-for-Success-Benchmarking-for-Continuous-Process-Improvement-508175/MARCH-2018-ES-TRAININGREGISTRY
  • 65 Request Info

    Webinar on Tools for Success: Developing a Demand-Driven Supply Chain Strategy

    Many manufacturing and distribution companies are moving from the traditional 'forecast push MRP' to demand-driven supply chain management (SCM). Demand-driven SCM is an 'end-to-end' supply chain planning and replenishment process that enables companies to achieve their planned service levels from up to half the average level of inventory and requiring significantly less throughput capacity - irrespective of the level of demand volatility or lead-time length. 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/Tools-for-Success-Developing-a-Demand-Driven-Supply-Chain-Strategy-504529/MARCH-2018-ES-TRAININGREGISTRY
  • 66 Request Info

    Webinar on Good Documentation Guideline (Chapter <1029> USP)

    This webinar will familiarize participants with USP Chapter <1029> on good documentation guidelines. This session will wrap up the general concept and will provide information as to what needs to be documented in certain records. 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-Guideline-Chapter-1029-USP-502613/MARCH-2018-ES-TRAININGREGISTRY
  • 67 Request Info

    Webinar on Writing Effective SOP’s for Quality Professionals: Best Practices for Life Science Companies

    This training program will guide attendees in writing effective Standard Operating Procedures and Work Instructions. It will also discuss how to assess and write to the audience and how to review and revise SOPs and Work Instructions. 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/Writing-Effective-SOP-s-for-Quality-Professionals-Best-Practices-for-Life-Science-Companies-504127/MARCH-2018-ES-TRAININGREGISTRY
  • 68 Request Info

    Webinar on Problem Solving - Root Cause Analysis in Pharma Manufacturing

    This topic will touch on investigations whether they are post-Audit, Deviation related, Complaints, etc. It will transition into determination of RCA, the many tools used during RCA & what they really are and how to use them to greater effect. 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/Problem-Solving-Root-Cause-Analysis-in-Pharma-Manufacturing-503456/MARCH-2018-ES-TRAININGREGISTRY
  • 69 Request Info

    Webinar on Understanding European Filing and Registration Procedures for Drug Approval

    Registration and applications within the European Union can follow various procedures depending on the type of product and the objectives of the sponsor. The pharmaceutical industry is one of the highly regulated industries, with many rules and regulations enforced by the government to protect the health and well-being of the public. Therefore, the aim of the pharmaceutical industry is to identify and develop a generic drug product which can be tailor made to meet the diverse market requirements. This webinar will review each type of application, when it is required and when it is recommended, along with pros and cons of each type.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/Understanding-European-Filing-and-Registration-Procedures-for-Drug-Approval-503328/MARCH-2018-ES-TRAININGREGISTRY
  • 70 Request Info

    Webinar on Drug Product Performance, In Vivo: Bioavailability and Bioequivalence

    Bioavailability is a measure of the rate and amount of drug that gets systemically absorbed and is available to the site of action. The ability to quantitate drug bioavailability and to compare drug bioavailability (bioequivalence) to different formulations of the same drug provides evidence that drug product performance is consistent and will produce a predictable therapeutic effect. 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/Drug-Product-Performance-In-Vivo-Bioavailability-and-Bioequivalence-507622/FEBRUARY-2018-ES-TRAININGREGISTRY
  • 71 Request Info

    Webinar on Get Lean, Not Mean - Secrets of the Toyota Production System

    The Toyota production system (TPS) originated at the Ford Motor Company during the first part of the 20th century was implemented and improved in Japan by Taiichi Ohno. Its focus is the elimination of waste (muda) from all aspects of manufacturing, and its principles extend into service operations (such as health care) as well. Deployment of the TPS has been proven to allow the simultaneous reduction of prices, increase in wages, and increase in profits, and therefore a win-win outcome for all supply chain stakeholders (relevant interested parties in ISO 9001). 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/Get-Lean-Not-Mean-Secrets-of-the-Toyota-Production-System-503735/FEBRUARY-2018-ES-TRAININGREGISTRY
  • 72 Request Info

    Webinar on Transform from Operations Laggard to Operations Leader

    Attendees will leave this meeting with a clear idea of where they stand, where they could be, and the justification for moving from operations laggard to leader. They also will hear many success stories, as well as the challenges involved in making the transition. This webinar is intended to answer the questions that lead to insights, justification, transition, and dramatic success. 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/Transform-from-Operations-Laggard-to-Operations-Leader-506943/FEBRUARY-2018-ES-TRAININGREGISTRY
  • 73 Request Info

    Webinar on Time Series Analysis Using MS Excel

    Medical device manufacturers must analyze complaints, process data, non-conformances, service records, internal quality audits, etc. This analysis, using appropriate statistical methodology under §820.100 and ISO 13485:2016, 8.4, identifies issues in the quality management system. The result can lead to corrective action and other improvement opportunities. 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/Time-Series-Analysis-Using-MS-Excel-502148/FEBRUARY-2018-ES-TRAININGREGISTRY
  • 74 Request Info

    Webinar on Implementation of a Successful Technology Transfer Process

    This training will introduce the concepts associated with implementing a carefully defined technical and business governance program along with clearly defined R&D to site transfer steps for successful implementation. It will cover the concepts associated with transferring the scientific technology needed to manufacture the product, processes to ensure the receiving manufacturing facility is ready for the product and tools and templates to help capture the knowledge. 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/Implementation-of-a-Successful-Technology-Transfer-Process-509919/FEBRUARY-2018-ES-TRAININGREGISTRY
  • 75 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
  • 76 Request Info

    Webinar on Modeling and Optimizing Process/Product Behavior Using Design of Experiments

    Experimentation is frequently performed using trial and error approaches which are extremely inefficient and rarely lead to optimal solutions. Furthermore, when it's desired to understand the effect of multiple variables on an outcome (response), "one-factor-at-a-time" trials are often performed. Not only is this approach inefficient, it inhibits the ability to understand and model how multiple variables interact to jointly affect a response. 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/Modeling-and-Optimizing-Process-Product-Behavior-Using-Design-of-Experiments-503135/JANUARY-2018-ES-TRAININGREGISTRY
  • 77 Request Info

    Webinar on Preparing a Proactive Root Cause Analysis with the Ishikawa Fishbone Tool

    What do you do next after you have found a non-conformance? Trying to do an uninformed 'fix' could do more harm than good, if we fix the wrong thing. All we'll do is damage the credibility of our corrective action processes and create doubts about our abilities to fix the weaknesses in our Management System. By using the Ishikawa Fishbone diagram we can take a structured approach to getting to the root of the problem. 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/Preparing-a-Proactive-Root-Cause-Analysis-with-the-Ishikawa-Fishbone-Tool-508166/JANUARY-2018-ES-TRAININGREGISTRY
  • 78 Request Info

    Webinar on Biopharmaceutic Considerations in Drug Product Design and In Vitro Drug Product Performance

    This webinar will demonstrate how biopharmaceutics may be used in the rational design of a drug product to achieve a desired therapeutic objective. Furthermore, the webinar will discuss the measurement of drug product performance, in vitro, including drug dissolution and in vitro in vivo correlation. 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/Biopharmaceutic-Considerations-in-Drug-Product-Design-and-In-Vitro-Drug-Product-Performance-502689/JANUARY-2018-ES-TRAININGREGISTRY
  • 79 Request Info

    Webinar on Spreadsheet Validation: Understanding and Satisfying FDA Requirements

    Many companies struggle with spreadsheet compliance. Some are still using invalidated spreadsheets. Many companies lack an understanding of how to satisfy FDA technical validation requirements as applied to spreadsheets. Most organizations lack a clear spreadsheet compliance strategy. An unplanned 'emergency' spreadsheet validation project could paralyze the organization. This webinar will describe methods for planning and executing spreadsheet validations that satisfy FDA requirements. 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/Spreadsheet-Validation-Understanding-and-Satisfying-FDA-Requirements-504170/JANUARY-2018-ES-TRAININGREGISTRY
  • 80 Request Info

    Webinar on Technical Writing in the Pharmaceutical Industry

    Technical writing in the Pharmaceutical Industry is a highly specialized field. Technical writing differs from general correspondence in that it is written for a specific audience. Technical writing is a balancing act between being precise enough to cover the subject matter yet general enough to apply to other situations and/or projects. It often consists of Standard Operating Procedures (SOPs) and reports but may apply to any documentation written for a restricted group. Technical writing always includes reviewers. 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/Technical-Writing-in-the-Pharmaceutical-Industry-509937/JANUARY-2018-ES-TRAININGREGISTRY