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  • 1 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
  • 2 Request Info

    Webinar on FDA Inspection: From SOP to 483

    This session will provide you guidance on how to prepare, behave and respond to an FDA inspection. 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/FDA-Inspection-From-SOP-to-483-503330/MARCH-2019-ES-TRAININGREGISTRY
  • 3 Request Info

    New National Bioengineered Food Disclosure Act (GMO Labeling)

    Learn about how to implement the new NBFDSA rule under GMO food labeling. Also meet the recordkeeping and compliance 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/New-National-Bioengineered-Food-Disclosure-Act-GMO-Labeling-509403/MARCH-2019-ES-TRAININGREGISTRY
  • 4 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
  • 5 Request Info

    Webinar on Principles of Lean Documents and Lean Configuration

    Learn how to create Design History Files, Device Master Records and Design History Files using lean document and lean configuration methods. 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/Design-History-File-DHF-the-Device-Master-Record-DMR-and-the-Device-History-Record-DHR-Principles-of-Lean-Documents-and-Lean-Configuration-505849/FEBRUARY-2019-ES-TRAININGREGISTRY
  • 6 Request Info

    Webinar on Implementing the ASTM E2500 Validation Method

    This validation training program will discuss regulatory requirements from the FDA, EU and ICH perspective, review all the detailed guidance on the concepts found in ASTM E2500 to help industry professionals understand how to implement a validation program based on the ASTM 2500 Approach. 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/Implementing-the-ASTM-E2500-Validation-Method-509460/FEBRUARY-2019-ES-TRAININGREGISTRY
  • 7 Request Info

    Webinar on IQ, OQ, PQ in the Verification and Validation Process

    Validation is an important element of the Quality System Regulations and ISO 13485. This course will cover what processes needed to be validated and what steps you need to take to validate processes. You'll also learn the essentials of validation planning, protocol writing, and change 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/IQ-OQ-PQ-in-the-Verification-and-Validation-Process-503996/FEBRUARY-2019-ES-TRAININGREGISTRY
  • 8 Request Info

    Webinar on Efficient and Effective Batch Record Reviews to Improve your Process Capabilities

    Understand regulatory requirements for batch record review and what to look for while reviewing batch records. Register for this webinar today. 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/Efficient-and-Effective-Batch-Record-Reviews-to-Improve-your-Process-Capabilities-506336/JANUARY-2019-ES-TRAININGREGISTRY
  • 9 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
  • 10 Request Info

    Webinar On Quality Control of Raw Materials (APIs and Excipients)

    A number of observations on FDA over the past several years reveal that pharmaceutical firms have not been performing adequate testing for incoming APIs, components and raw materials. The regulatory requirements are defined in the GMPs. Because of recognized problems in the incoming material supply chains, the agency is placing more emphasis on material quality. If you make such observations as your base, it appears that some organizations have chosen to ignore/misinterpret the regulatory expectations.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/QUALITY-CONTROL-OF-RAW-MATERIALS-APIS-505020/NOVEMBER-2017-ES-TRAININGREGISTRY
  • 11 Request Info

    Webinar On Principles of 21 CFR Part 820 Quality System Regulations

    All life science businesses are required to maintain their Quality Management System (QMS) processes in a state of control, via controlled documents and objective evidence in the form of records. Medical device manufacturing plants, required to follow 21 CFR Part 820, have the additional responsibility to ensure that each and every step of the manufacturing process is controlled by work instructions, SOPs, set-up instructions, equipment maintenance, and support functions, and that evidence of this work is maintained by controlled records.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://onlinecompliancepanel.com/webinar/21-CFR-PART-820-QUALITY-SYSTEM-REGULATION-506042/NOVEMBER-2017-ES-TRAININGREGISTRY
  • 12 Request Info

    Webinar On Implementing a Metrics Program - Uncovering and Overcoming the Challenges

    Recently the FDA released their draft guidance for industry entitled "Request for Quality Metrics". Much discussion of quality metrics has ensued regarding this guidance and its elements. This presentation provides an integrated view of the aspects of Quality Metrics including the required supporting quality culture..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/METRICS-PROGRAM-503090/AUGUST-2017-ES-TRAININGREGISTRY
  • 13 Request Info

    Webinar On Top Process Validation Mistakes - And How to Avoid Them

    Validation is an important element of the Quality System Regulations and ISO13485. This course will cover the essentials of validation. You’ll learn about what processes needed to be validated and what steps you need to take to validate processes. You’ll learn the essentials of validation planning, protocol writing, and change management. We’ll cover the steps of Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) including tips and best practices. We’ll discuss the top mistakes that companies make and how you can avoid them..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/TOP-PROCESS-VALIDATION-MISTAKES-509627/AUGUST-2017-ES-TRAININGREGISTRY
  • 14 Request Info

    Webinar On Ensure Compliance to FDA's Design Control by using Requirements Management Techniques

    This webinar on FDA's design control requirements will discuss how a requirements management approach consistent with the CMMi requirements management KPA, helps companies meet FDA's design control 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/COMPLIANCE-FDAs-DESIGN-CONTROL-504040/AUGUST-2017-ES-TRAININGREGISTRY
  • 15 Request Info

    Webinar On Conducting a Software Validation of Medical Device to Meet FDA Requirements

    This course will teach how to conduct a software validation program that will satisfy FDA requirements and produce a safe product. We will explain the role of risk analysis in validation. How software requirements are used in validation will be described. This course is not a programming course. We will discuss what must be done but will not discuss methods to execute necessary testing.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/SOFTWARE-VALIDATION-MEDICAL-DEVICE-501884/NOVEMBER-2016-ES-TRAININGREGISTRY
  • 16 Request Info

    Webinar On Quality Metrics Program: FDA Challenges and Requirements including the New 'Quality Metrics Technical Conformation Guide' Released June 201

    The Food, Drug and Cosmetic Act of 1938 as revised by the Food and Drug Administration Safety and Innovation Act (FDASIA) of 2014, gives the FDA the authority to require the reporting of Quality Metrics. In July 2015 the FDA issued a draft guidance, 'Request for Quality Metrics' in which the Agency shared its plan to require all firms that market a drug substance or drug product in the U.S. to provide specific data to the FDA which it will use to calculate defined quality metrics.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/QUALITY-METRICS-PROGRAM-501727/SEPTEMBER-2016-ES-TRAININGREGISTRY
  • 17 Request Info

    Webinar On How to use Risk Based Process Safety's skills to be in compliance with ICH-Q9 "Quality Risk Management" in the Pharmaceutical Industry

    This webinar will cover the similarities between the second pillar "Knowing the Process" of the Risk Based Process Safety Management and ICH-Q9 "Quality Risk Analysis". This webinar will provide the tools and help to identify the process required information to perform the quality risk by using methodologies in the process hazard analysis (PHA) to determine possible deviation during the process to achieve the good quality of the finished product.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/QUALITY-RISK-MANAGEMENT-PHARMACEUTICAL-INDUSTRY-501651/SEPTEMBER-2016-ES-TRAININGREGISTRY
  • 18 Request Info

    Webinar On Risk Based Approach for Medical Device Design Control

    This course will explain how to manage a Design Control program that will meet FDA requirements and minimize chances of your medical device being recalled. Such a program will also help to get projects completed on time and within budget. The important and confusing question of when, in a development process, Design Control begins will be answered. The difference between pre-release and post release change control will be explained.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/RISK-BASED-APPROACH-MEDICAL-DEVICE-DESIGN-501511/AUGUST-2016-ES-TRAININGREGISTRY
  • 19 Request Info

    Webinar On Enhancing your CAPA Program by Developing a Learning Organization

    This Webinar provides tools needed to sell a meaningful CAPA program up to Management, by discussing how CAPA can be used as a tool to yield business results. This well-researched webinar references classic business literature, written by famous business minds, such as Peter Drucker and Peter Senge, to describe how a CAPA program appeals to the needs of Knowledge Workers in a Learning Organization, CAPA therefore becomes a business tool to un-learn behaviors that are thwarting progress in the organization, and becomes a tool for sustainable change, organization alignment and business risk management.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/ENHANCING-CAPA-PROGRAM-LEARNING-ORGANIZATON-501459/JUNE-2016-ES-TRAININGREGISTRY
  • 20 Request Info

    Webinar OGMPs for OTC and Cosmetic Products - US and Global Requirementsn

    The cosmetic good manufacturing practice is a set of manufacturing guidelines to ensure the safety and quality of cosmetic products. OTC drug manufacturers, labelers, packagers and holders must comply with good manufacturing practices.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/GMPS-OTC-COSMETIC-PRODUCTS-501385/MAY-2016-ES-TRAININGREGISTRY