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Courses

  • 1 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
  • 2 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
  • 3 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
  • 4 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
  • 5 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
  • 6 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
  • 7 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
  • 8 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
  • 9 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
  • 10 Request Info

    Webinar on Effective and Practical use of FMEA For Risk-Based Approach to Computer Systems Validation

    Validation of computer systems is a regulatory requirement within the life sciences. "How much to validate" is one of the biggest challenges validation teams face. The struggle to balance time and available resources with compliance requirements often leads to insufficient testing and/or project overruns, which in turn can lead to significant regulatory and safety risks. 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/Effective-and-Practical-use-of-FMEA-For-Risk-Based-Approach-to-Computer-Systems-Validation-503169/AUGUST-2018-ES-TRAININGREGISTRY
  • 11 Request Info

    Webinar on Applying Global Standards to Life Sciences Compliance Documentation

    Learn how to write SOP and work instructions and explore the true purpose and function of compliance documents. 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/Applying-Global-Standards-to-Life-Sciences-Compliance-Documentation-504874/AUGUST-2018-ES-TRAININGREGISTRY
  • 12 Request Info

    Webinar on Comply US Customs Importing Requirements and the MOD Act

    Attend this introductory trade logistic session that provide valuable assistance to corporate import team and give company the tools to assess potential gaps. 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/Complying-with-Customs-laws-and-Responsibilities-under-the-Customs-Modernization-Act-507252/AUGUST-2018-ES-TRAININGREGISTRY
  • 13 Request Info

    Webinar on Refuse to Accept (k) and Acceptance Reviews for PMAs Guidance

    This webinar will notify how US FDA updated its PMA acceptance process and refuse to accept policy for initial reviews of (k) submissions. 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-the-FDA-s-Revised-Medical-Device-Product-Guidance-Refuse-to-Accept-Policy-for-510-k-s-and-Acceptance-and-Filing-Reviews-for-Premarket-Approval-Applications-PMAs-503623/JULY-2018-ES-TRAININGREGISTRY
  • 14 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
  • 15 Request Info

    Managing Risk for Medical Devices in Compliance with ISO 14971

    Join this webinar to understand how Risk Management applies throughout the product life cycle and links to design control, production and process controls, and CAPA. 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/Risk-Management-Techniques-for-Medical-Devices-506211/JULY-2018-ES-TRAININGREGISTRY
  • 16 Request Info

    Design of Experiments Strategies | Six Sigma Process

    Join this webinar Design of experiments "DOE" which is a systematic method to determine the relationship between factors affecting a process and the output of that process. 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/Effective-Design-of-Experiments-DOE-Strategies-503955/JULY-2018-ES-TRAININGREGISTRY
  • 17 Request Info

    Webinar on AS9100:2016 Rev D Transition: Key Changes You Need To Know Before Sep 2018

    Attend this webinar you ll be able to identify the gaps in your current Aerospace Quality Management Systems AQMS and start planning your transition to the revised standard. 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/AS9100-2016-Rev-D-Transition-Key-Changes-You-Need-To-Know-Before-Sep-2018-509894/JULY-2018-ES-TRAININGREGISTRY
  • 18 Request Info

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

    Know everything about 21 CFR Part 11 compliance and how to control electronic signatures and electronic 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/21-CFR-Part-11-Electronic-Record-and-Signature-Validation-508215/JULY-2018-ES-TRAININGREGISTRY
  • 19 Request Info

    Webinar on Process Validation - Overview of Why and How

    Attend this webinar to gain an understanding of FDA and ISO 13485 requirements for process validation and how to implement them. 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-Validation-Overview-of-Why-and-How-507096/JULY-2018-ES-TRAININGREGISTRY
  • 20 Request Info

    Webinar on Reliability Engineering Fundamentals for Medical Devices

    This webinar will cover the science and techniques for designing highly reliable medical devices at lower cost and in lesser time. 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/Reliability-Engineering-Fundamentals-for-Medical-Devices-503951/JULY-2018-ES-TRAININGREGISTRY