Manufacturing Skills - Management

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  • 61 Request Info

    Webinar on Common Problems and Mistakes in Method Validation in Drug Development Process

    This webinar provides information that will identify and correct common issues that may arise during validation of methods required in drug development. 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/Common-Problems-and-Mistakes-in-Method-Validation-in-Drug-Development-Process-505094/JULY-2018-ES-TRAININGREGISTRY
  • 62 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
  • 63 Request Info

    Webinar On Complaints, Servicing and FDA Reporting

    This presentation provides a framework for understanding, managing, and reporting adverse events to the FDA. It uses plain English to describe the regulatory requirements as well as common quality tools such as flow diagrams and fault tree analysis. This approach helps participants understand and implement the essential parts of the regulations.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/COMPLAINTS-SERVICING-FDA-REPORTING-507863/JUNE-2017-ES-TRAININGREGISTRY
  • 64 Request Info

    Webinar On Compliance Secrets from a Former Customs Officer

    What common importer or customs broker mistakes get unwanted scrutiny from U.S. Customs and Border Protection? What are the smartest steps that an importer should take to avoid shipment delays, requests for delays, detentions, seizures, and penalties/liquidated damages? This webinar is unique because it will be delivered by a practicing attorney not only for his expertise with customs law compliance, but also a former officer with CBP.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/COMPLIANCE-SECRETS-FORMER-CUSTOMS-OFFICER-502190/JULY-2017-ES-TRAININGREGISTRY
  • 65 Request Info

    Webinar on Controlling Human Error in the Manufacturing Floor

    This online training session would provide practical tools that can be implemented and used for controlling human error in the manufacturing floor. The webinar will also discuss human error categories, near root causes, root causes for these events and latest trends in human error issues in the industry. 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/CONTROL-HUMAN-ERROR-501192/JAN-2016-ES-TRAININGREGISTRY
  • 66 Request Info

    Webinar on Controlling Human Error in the Manufacturing Floor

    This webinar will discuss about human error factors & performance issues and also how to implement practical tools to prevent/reduce the human error rates. 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/Controlling-Human-Error-in-the-Manufacturing-Floor-504173/FEBRUARY-2019-ES-TRAININGREGISTRY
  • 67 Request Info

    Webinar On Creating a Good Design History File (DHF) for Audit Success

    This webinar will cover the basics on how to maintain a good Design History File (DHF) that will help a manufacturer in a regulatory compliance audit. The webinar will cover the structure of a DHF and steps to ensure that the DHF is completed as the design and development process progresses. The DHF needs to be maintained as design changes are performed. Information in the DHF can help facilitate design decisions, which often can affect the safety of the device. The DHF provides the knowledge base needed for the manufacturer to maintain the device. It also provides the secrets to a successful Design Control audit.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-DESIGN-HISTORY-FILE-AUDIT-506688/JULY-2017-ES-TRAININGREGISTRY
  • 68 Request Info

    Webinar On Creating an Effective Contamination Control & Environmental Monitoring Program

    This webinar will provide an overview of environmental monitoring and provide aspects of contamination control. 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.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-MONITORING-PROGRAM-501909/DECEMBER-2016-ES-TRAININGREGISTRY
  • 69 Request Info

    Webinar On Customs-Trade Partnership Against Terrorism (C-TPAT) and Supply Chain Security

    You should attend this training if you have a role in a manufacturing or freight/shipping company that handles goods distributed globally. The training will help you secure the international supply chain and mitigate the risks associated with illegal activities that support and fund terrorism.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/C-TPAT-SUPPLY-CHAIN-SECURITY-501467/AUGUST-2016-ES-TRAININGREGISTRY
  • 70 Request Info

    Webinar On Data Analysis in QSR

    Data analysis is one of the most powerful improvement tools because it can lead to cost reductions and preventive action. To use these techniques you need to know both the regulatory requirements and the analysis framework. This presentation provides that essential information.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/DATA-ANALYSIS-QSR-507590/MARCH-2017-ES-TRAININGREGISTRY
  • 71 Request Info

    Webinar on Data Governance for Computer Systems Regulated by FDA

    The attendees will learn how to leverage best practices across all systems by creating a standardized program for FDA data governance. 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/Data-Governance-for-Computer-Systems-Regulated-by-FDA-502212/APRIL-2018-ES-TRAININGREGISTRY
  • 72 Request Info

    Webinar on Data Governance for Computer Systems Regulated by FDA

    The attendees will learn how to leverage best practices across all systems by creating a standardized program for FDA data governance. 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/Data-Governance-for-Computer-Systems-Regulated-by-FDA-502212/MAY-2018-ES-TRAININGREGISTRY
  • 73 Request Info

    Webinar On Demonstrating Product Reliability - Sample Sizes and Testing Times

    Product Reliability requirements must be satisfied like all other performance requirements prior to product launch. However, since reliability is a function of time, the methods for verifying that reliability performance has been verified differ than for most other performance characteristics. This webinar will present several approaches for verifying that reliability targets or specifications have been achieved at the desired level of confidence. Specifically, approaches using time-to-failure data to estimate reliability metrics as well as demonstration tests, where minimum reliability may be demonstrated with zero or few failures are discussed.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/DEMONSTRATING-PRODUCT-RELIABILITY-508137/JULY-2017-ES-TRAININGREGISTRY
  • 74 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
  • 75 Request Info

    Webinar on Developing Effective Risk Management Policies To Ensure Your Company’s Compliance with the Foreign Corrupt Practices Act

    This risk management training discusses about developing effective policies to ensure company’s compliance with the Foreign Corrupt Practices Act. 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/Developing-Effective-Risk-Management-Policies-To-Ensure-Your-Company-s-Compliance-with-the-Foreign-Corrupt-Practices-Act-502802/MAY-2018-ES-TRAININGREGISTRY
  • 76 Request Info

    Webinar on Downsizing: Best Practices and Beyond

    This webinar focus on effective organizational downsizing strategies as well as the impact on employees who are laid off or those employees who remain. 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/Downsizing-Best-Practices-and-Beyond-509200/APRIL-2018-ES-TRAININGREGISTRY
  • 77 Request Info

    Webinar On Drive Continuous Improvement with Shingo Maps and ISO 9001:2015

    Shingo process maps were developed originally to support kaizen events and other improvement events. They can, however, support managed continual improvement along with ISO 9001:2015's requirement (7.5) for documented information; a common role of the traditional process flowchart.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/SHINGO-MAPS-ISO-9001-2015-501917/DECEMBER-2016-ES-TRAININGREGISTRY
  • 78 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
  • 79 Request Info

    Webinar On Effective Corrective and Preventive Action Program (CAPA): The Role of Corrective Action and Preventative Action in Your Quality Management

    Corrective and Preventive Actions (CAPAs) are a beneficial tool for documenting potential problems and investigating them through root cause analysis. Today, more companies are utilizing CAPAs to properly document investigations and capture the action taken by the company. This session will cover the CAPA process, how to implement an effective CAPA system using a risk-based approach and review the key elements of a CAPA report.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/CORRECTIVE-PREVENTIVE-ACTION-PROGRAM-CAPA-501961/DECEMBER-2016-ES-TRAININGREGISTRY
  • 80 Request Info

    Webinar On Effective Purchasing and Supplier Controls for Medical Device Manufacturers

    This webinar can help you understand your responsibilities in terms of Purchasing Controls enabling you to provide safe and effective products to your customers. Learn how to prevent quality and compliance problems by having a strong system for Purchasing Controls! This webinar will help you to understand the regulations and how you can translate them into an efficient and effective process for purchasing/ supplier control.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/PURCHASING-SUPPLIER-CONTROLS-505726/APRIL-2017-ES-TRAININGREGISTRY