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Courses

  • 1 Request Info

    Webinar on How to Prepare for FDA Inspections and Customer Audits of Pharmaceuticals

    Learn how to prepare for an FDA inspection and how to behave during one by attending this webinar by Dr. Loren Gelber. Register Today. 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/How-to-Prepare-for-FDA-Inspections-and-Customer-Audits-of-Pharmaceuticals-505331/May-2019-ES-TRAININGREGISTRY
  • 2 Request Info

    Webinar on Test Method Validations for Medical Devices

    This webinar will help you have an understanding of successful Test Method Validation and the detailing of real-life case studies. 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/Test-Method-Validation-to-Verify-your-Device-Performance-503591/May-2019-ES-TRAININGREGISTRY
  • 3 Request Info

    Webinar on Guidance on Elemental Impurities - According to ICH Q3D & USP 232/233

    Learn about elemental impurities either through thorough risk assessments or through testing. And it will provide an understanding of the standards and guidelines. 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/Elemental-Impurities-Tests-for-Pharmaceutical-Products-according-to-the-ICH-Q3D-and-USP-232-233-Guidelines-507031/APRIL-2019-ES-TRAININGREGISTRY
  • 4 Request Info

    Webinar on Medical Device Complaints & CAPA

    Attend this webinar to learn the most important areas of medical device safety and how complaint handling and CAPA process is used during FDA inspections. 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/Medical-Device-Complaints-CAPA-506097/APRIL-2019-ES-TRAININGREGISTRY
  • 5 Request Info

    Webinar on New Safe Foods for Canadians Regulation

    Learn all the new SFCR rules which focus on food safety needs along with avoiding penalties by complying with the regulations. 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/New-Safe-Foods-for-Canadians-Regulation-508013/APRIL-2019-ES-TRAININGREGISTRY
  • 6 Request Info

    Webinar on Cleaning Validations Using Extraction Techniques

    This webinar will provide valuable guidance on how to use extraction techniques to validate the cleanliness of a device. 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/Cleaning-Validations-Using-Extraction-Techniques-504912/MARCH-2019-ES-TRAININGREGISTRY
  • 7 Request Info

    Webinar On From NAFTA to USMCA - Key differences

    Learn the key differences between NAFTA and USMCA, legal requirements, and the custom clearance process. 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/From-NAFTA-to-USMCA-Key-differences-505468/MARCH-2019-ES-TRAININGREGISTRY
  • 8 Request Info

    Webinar on 21 CFR Part 11 - Electronic Record and Signature Validation

    This session will provide you information with procedures for controlling electronic signatures and electronic records and how 21 CFR Part 11 is connected with this area. 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/21-CFR-Part-11-Electronic-Record-and-Signature-Validation-509394/MARCH-2019-ES-TRAININGREGISTRY
  • 9 Request Info

    Webinar on Understanding QbD Approach to Analytical Method Lifecycle

    This webinar is designed to provide participants with a lifecycle approach to developing and validating analytical methods and comply with compendial requirements. 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/QbD-Approach-to-Analytical-Method-Lifecycle-Design-Development-Validation-Transfer-504438/MARCH-2019-ES-TRAININGREGISTRY
  • 10 Request Info

    Webinar on Analytical Method Validation and Transfer

    This course provides guidance on tools to plan and execute test method validation and transfer also a comprehensive overview of the international regulatory authority requirements. 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/Analytical-Method-Validation-and-Transfer-506228/MARCH-2019-ES-TRAININGREGISTRY
  • 11 Request Info

    Webinar on Tobacco Industry Trends for Computer Systems Regulated by FDA

    Get an overview of the regulations as they pertain to the manufacturing, marketing, distribution and other operational activities engaged by companies in the tobacco industry. This course will describe the best practices for developing a compliance strategy, including roles and responsibilities, and the policies and procedures that should be followed to ensure compliance.Price:$150.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Tobacco-Industry-Trends-for-Computer-Systems-Regulated-by-FDA-508423/JANUARY-2019-ES-TRAININGREGISTRY
  • 12 Request Info

    Webinar on Best Practice Case Management Roles and Functions: How to Optimize RN and Social Worker Skill Sets

    Due to the variety of differences in the definition of case management and roles and functions, there is much confusion in the field as to what case management is and how it is applied. Without a national perspective on this issue, many case management departments are not designed to respond to the challenges of health care reform. 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/Best-Practice-Case-Management-Roles-and-Functions-How-to-Optimize-RN-and-Social-Worker-Skill-Sets-504932/NOVEMBER-2018-ES-TRAININGREGISTRY
  • 13 Request Info

    Webinar on Establishing a Robust Supplier Management Program

    Regulatory expectations are clear about manufactures' responsibility regarding supplier quality oversight. All regulatory agencies agree that pharmaceutical and medical device manufactures are responsible for ensuring their suppliers adhere to quality standards, maintain compliance to regulatory requirements and consistently meet established 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/Establishing-a-Robust-Supplier-Management-Program-505529/NOVEMBER-2018-ES-TRAININGREGISTRY
  • 14 Request Info

    Webinar on Process Capability Assessment for Normal and Non-Normal Data

    This webinar discusses methods for estimating process capability for both normal and non-normal data. Pre-requisites for estimating process capability (e.g. establishing process stability) are discussed first. Distributions are briefly described and methods for estimating ppm levels are presented. 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-Assessment-for-Normal-and-Non-Normal-Data-503555/NOVEMBER-2018-ES-TRAININGREGISTRY
  • 15 Request Info

    Webinar on Managing the FDA form "483": Inspection Observations

    FDA inspections look for noncompliance with applicable manufacturing regulations. During the inspection the FDA investigator makes a "list of observations" that gives examples of violations. The list is known as the "483." Some observations are very serious and can easily lead to receiving a Warning Letter, which threatens legal action. Your response to a 483 plays a critical role in how the agency will evaluate the inspection. A poorly written response or not responding at all will certainly lead to a Warning Letter and follow up action by FDA. 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/Managing-the-FDA-form-483-Inspection-Observations-503502/SEPTEMBER-2018-ES-TRAININGREGISTRY
  • 16 Request Info

    Webinar on Mobile Applications and Computer Systems Regulated by FDA

    This topic is focused on the use of mobile applications to process data regulated by FDA. These applications may be used to collect, analyze, transfer, report, or otherwise manage data that will be submitted to FDA and/or must be available for FDA review upon inspection or 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/Mobile-Applications-and-Computer-Systems-Regulated-by-FDA-508531/SEPTEMBER-2018-ES-TRAININGREGISTRY
  • 17 Request Info

    Webinar on Regulatory Inspections - How to prepare for a visit from an FDA auditor

    This FDA audit webinar will highlight the purpose of FDA audits and scope, understanding of QSIT audit and how to develop an audit preparedness plan. It will also give understanding of what the FDA will look for at the conclusion of your audit and how to communicate with FDA before and after the 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/Regulatory-Inspections-How-to-prepare-for-a-visit-from-an-FDA-auditor-506970/SEPTEMBER-2018-ES-TRAININGREGISTRY
  • 18 Request Info

    Webinar on Integration Management - The Project Managers Key Role

    In this webinar we stress the project manager integration roles: how their product integrates to the customer's suite, how their team integrates into the operational staff, and how new technology integrates with their product. 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/Integration-Management-The-Project-Managers-Key-Role-504229/SEPTEMBER-2018-ES-TRAININGREGISTRY
  • 19 Request Info

    Webinar on Residual Solvents: Take Advantage of the New Flexibility in Revised USP <467>

    This training on residual solvents will discuss the regulatory landscape for residual solvents and compliance requirements, including interpretation of the majors' sections (classes of solvents, options for describing levels, analytical procedures).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/Residual-Solvents-Take-Advantage-of-the-New-Flexibility-in-Revised-USP-467-507766/AUGUST-2018-ES-TRAININGREGISTRY
  • 20 Request Info

    Webinar on Sampling - How Large a Sample Do I Need? Determining the Right Size for Accurate, Cost Effective Results

    The Pharmaceutical and Biotech industries are going through tremendous changes that have been increased by the recent global financial challenges. The FDA is promoting the use of Quality-by-Design (QbD) as an approach for helping companies speed up development and improve their operations. 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/Sampling-How-Large-a-Sample-Do-I-Need-Determining-the-Right-Size-for-Accurate-Cost-Effective-Results-506454/AUGUST-2018-ES-TRAININGREGISTRY