Manufacturing Skills - Management

If you can't find what you want, Ask Us.

Refine Your Results

reset

Filter by Category

Location

Dates

FEATURED VENDORS

Showing 81-100 of 211 results Sort by:

Courses

  • 81 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
  • 82 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 ยง820.100 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
  • 83 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
  • 84 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
  • 85 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
  • 86 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
  • 87 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
  • 88 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
  • 89 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
  • 90 Request Info

    Auditing and Inspecting Preclinical Research for GLP Compliance

    The Good Laboratory Practice (GLP) guidelines have progressed through various transitional phases to become guidelines in some countries and regulatory/statutory instruments in others. The objective of the GLPs is to ensure that a standard approach is undertaken, covering traceability and accountability of medical research and drug development process. This webinar discusses various aspects of auditing and inspecting preclinical research compliance with GLP. 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/Auditing-and-Inspecting-Preclinical-Research-for-GLP-Compliance-503774/DECEMBER-2017-ES-TRAININGREGISTRY
  • 91 Request Info

    Webinar on Good Manufacturing Practices for Active Pharmaceutical Ingredients (APIs)

    This webinar will cover ICH Q7, Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients (API). Attendees will gain a deeper understanding of the importance of GMPs for APIs, apply these principles in their current roles in order to better manage quality, make improvements, solve problems and make decisions. 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-Manufacturing-Practices-for-Active-Pharmaceutical-Ingredients-APIs-509253/DECEMBER-2017-ES-TRAININGREGISTRY
  • 92 Request Info

    Webinar on Developing an Effective CAPA Management and Root Cause Analysis System

    This 90-minute webinar will include discussions on proper CAPA system maintenance, root cause analysis, documentation of the Corrective and Preventative Actions and developing a robust CAPA plan. It will give tips on how to develop CAPAs pertaining to longer term projects and ensure they stay on track. 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/Developing-an-Effective-CAPA-Management-and-Root-Cause-Analysis-System-503423/DECEMBER-2017-ES-TRAININGREGISTRY
  • 93 Request Info

    Cleaning Validations Using Extraction Techniques

    Cleaning validations are an essential step in the medical device development process. One of the most common methods is using extraction techniques to validate the cleanliness of a device. This webinar will provide valuable guidance on how to achieve a thorough validation of a cleaning process. These cleaning processes may include initial cleaning validations, in process cleaning validations, or reprocess cleaning validations.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/Cleaning-Validations-Using-Extraction-Techniques-507793/DECEMBER-2017-ES-TRAININGREGISTRY
  • 94 Request Info

    Webinar on Labeling, Advertising and Promotion in a Regulated Environment

    The changing game for drug and device marketing, however, is governed by antiquated and inadequate rules created for traditional print and broadcast advertising by the Food and Drug Administration ("FDA"). How the FDA will deal with such advanced communication technology that can go "viral" and just as quickly disappear is the question that the industry is eager to have answered. 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/LABELING-ADVERTISING-AND-PROMOTION-IN-A-REGULATED-ENVIRONMENT-504242/NOVEMBER-2017-ES-TRAININGREGISTRY
  • 95 Request Info

    Webinar on Regulatory and Testing Requirements of the Bacterial Endotoxin Testing (BET) or LAL Program

    cGMP drug products rely on the bacterial endotoxin test as a critical release test for products based on the route of administration of the drug product. Having a good concept of this critical release assay, its application and importance to the manufacture of cGMP product is valuable so as to avoid costly errors, batch disposal, expensive failure investigations and delays in the release of products that some manufacturers have undergone. 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/REGULATORY-AND-TESTING-REQUIREMENTS-OF-THE-BACTERIAL-ENDOTOXIN-TESTING-BET-OR-LAL-PROGRAM-507120/NOVEMBER-2017-ES-TRAININGREGISTRY
  • 96 Request Info

    Webinar on Qualification of Contract Manufacturer Organizations Based on Practical Experience

    This webinar will cover in detail the steps to plan and conduct a program to qualify contract manufacturer organizations (CMOs). It will teach best practices to meet regulatory requirements and satisfy practical needs to obtain the best CMO. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://onlinecompliancepanel.com/webinar/QUALIFICATION-OF-CONTRACT-MANUFACTURER-ORGANIZATIONS-505388/NOVEMBER-2017-ES-TRAININGREGISTRY
  • 97 Request Info

    LEADERSHIP ESSENTIALS FOR TEAM LEADERS & SUPERVISORS

    Click on the name of the course to be taken to our website for class schedule, class outline, and to register. In this Leadership Essentials course, you will learn how to establish direction for your team and to influence and align them toward the company's goals, motivating and committing them to action and making them responsible for their performance.
  • 98 Request Info

    Design Controls for Medical Devices - Regulations, Myths, Challenges, and Best Practices 2017

    Design Controls are essential for producing safe and effective medical devices. And Design Controls are considered a critical process by the FDA. Yet is still one of the most frequent areas for 483 and Warning Letter observations. This 2 days seminar will help you understand and develop design controls processes and tools that are a competitive strength for your company. Intrinsic quality, safety, and effectiveness of a device are known to be established during the design phase. Yet, statistics show that a significant percentage of all medical device recalls are due to design problems. And design problems can have disastrous results for your customer and for your company.
  • 99 Request Info

    The DHF, DMR, DHR, and Technical File - Design Dossier 2017

    We will consider the following: The Design Control requirements of the CGMPs, 21 CFR 820.30 The Design History File - documenting Product Design Control and its nine elements The Device Master Record and the Device History Record The EU's Medical Device Directive The "Essential Requirements"; and their documentation The remaining elements of a Technical File / Design Dossier Trends Two attendee projects
  • 100 Request Info

    Webinar On Mexican Import Process

    Since the implementation of NAFTA, Mexico has become a major market for USA exporters. This course will provide an in-depth explanation of the Mexican importing process, including specific rules and documentation. The webinar will also discuss what impact local government and private resources will have on the exporter's transaction process when it comes to tariff costs in this trading environment.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/MEXIAN-IMPORT-PROCESS-505340/AUGUST-2017-ES-TRAININGREGISTRY