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Courses

  • 1 Request Info

    Creation of DHFs, DMRs, and DHRs utilizing the principles of Lean Documents and Lean Configuration

    The Theory of Lean Documents is the product of applying lean principles to the creation, design, process, and management of controlled documents typically found in regulated industries. Just as lean principles challenge traditional process concepts and "push" systems, many traditional document practices are artefacts of a flawed approach. Lean documents presents a fresh departure from these practices, while building upon proven principles. Lean configuration comes from the same principles, utilizing the unique power of software solutions to take over functions that had previously burdened controlled "paper" documents.
  • 2 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
  • 3 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
  • 4 Request Info

    Introduction to Design of Experiments

    Design of Experiments is a vital tool for process improvement and root cause analysis. It allows experimenters to determine beyond a quantifiable reasonable doubt that an experiment improves the process, or that there is a difference between treatments; choices among the factors of the cause and effect diagram. While comprehensive mastery of DOE requires full college-level courses, enough basics can be taught in an hour to enable the attendee to know the key considerations in the design of an experiment, and also interpretation of its results. The material on hypothesis testing will also position the attendee to understand statistical process control (SPC) and acceptance sampling.
  • 5 Request Info

    Kano Analysis for Product Decisions

    Kano Analysis, an important tool for product development, uses a structured methodology to help determine important device characteristics. For example, if customers expect a device will have a certain feature, they would be disappointed if it isn't there. However, if it were there, it doesn't create satisfaction; it was assumed.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/Kano-Analysis-for-Product-Decisions-508099/JANUARY-2018-ES-TRAININGREGISTRY
  • 6 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
  • 7 Request Info

    Managing Risks in High-Stakes Projects

    Builds practical skills in using tools & techniques to identify the sources of uncertainty that give rise to risks in high-stakes projects. Also, how to isolate and absorb the uncertainty factors to limit their potential impact. See online description for additional details.
  • 8 Request Info

    Process Capable Tolerancing® (PCT) Training

    1 Day Who should attend: Designers, Design Engineers and those involved with supplier selection. The statistical concepts behind the process capability index Cpk and its importance to the engineers and designers will be explained in layman's terms. After presenting an introduction to tolerance stack up using the vector method, the Process Capable Tolerancing™ (PCT) methodology for creating components and products that are robust to process variation is presented. The Tolerance Capability Expert™ (TCE) software which facilitates the application of this methodology is demonstrated. The methodology is illustrated through industrial case studies
  • 9 Request Info

    Risk Based Approach to Environmental Monitoring

    Regulators frequently cite concerns with environmental monitoring and the lack of a well-thought out rationale. This shortfall can be overcome through the application of risk assessment and scientific approaches. The application of risk assessment applies to selecting location for monitoring and frequencies of monitoring; and for data assessment. This presentation outlines the primary tools that can be used to achieve this.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/Risk-Based-Approach-to-Environmental-Monitoring-504486/DECEMBER-2017-ES-TRAININGREGISTRY
  • 10 Request Info

    Risk Based Thinking in and Beyond ISO 9001:2015

    ISO 9001:2015's new clause for "actions to address risks and opportunities" is among the biggest revisions to the standard. Risks and opportunities that relate to waste or muda, and also to changes in technology, markets, and distribution channels are however not explicitly covered, and are therefore not explicitly auditable, even under the new standard. This credit risk mitigation presentation will therefore focus on use of the standard as a servant whose purpose is to promote the organization's competitiveness and profitability, rather than a master whose requirements the organization has to satisfy to get the ISO certificate. ISO 9001 becomes the servant when the organization uses it as a framework to drive continual improvement and to identify risks and opportunities that lie well beyond the scope of the standard.
  • 11 Request Info

    Two Days Workshop On Statistical Analysis for Process and Product Development

    This course is designed to help scientists and engineers apply statistical methods used to assist decision making in process and product development. Variability must be considered when utilizing data to arrive at conclusions. This course will cover Basic Statistics and Graphical Methods used to summarize data. You will learn how to apply Hypothesis Testing methods to determine whether groups are statistically equivalent or not with respect to key process characteristics such as process averages and variability. Single Registration :- $1,400.00 http://www.onlinecompliancepanel.com/workshop/STATISTICAL-ANALYSIS-800008/APRIL-2016-ES-TRAININGREGISTRY
  • 12 Request Info

    Webinar On 21 CFR Part 11 - Electronic Record and signature Validation

    This Webinar will explain what 21 CFR Part 11 is, why it is important to FDA regulated companies and how conformance to Part 11 differs from just having good IT security. Procedures for controlling electronic signatures and electronic records 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://www.onlinecompliancepanel.com/webinar/21-CFR-PART-11-ELECTRONIC-RECORD-SIGNATURE-VALIDATION-501462/JUNE-2016-ES-TRAININGREGISTRY
  • 13 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
  • 14 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
  • 15 Request Info

    Webinar on Acceptance Activities in FDA's Quality Management System

    Understand how purchasing and acceptance activities are linked and combine to facilitate effective supplier 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/Acceptance-Activities-in-FDA-s-Quality-Management-System-507314/APRIL-2018-ES-TRAININGREGISTRY
  • 16 Request Info

    Webinar On Acceptance Sampling Plans for Process Validation and Production Lot Monitoring

    This webinar will cover acceptance sampling plans for process validation and production lot acceptance. Sampling plans for attribute data are the primary focus although variable acceptance sampling plans are presented as well. The binomial distribution and its use in developing Operating Characteristic (OC) curves will be discussed.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/PROCESS-VALIDATION-PRODUCTION-LOT-MONITORING-501949/JANUARY-2017-ES-TRAININGREGISTRY
  • 17 Request Info

    Webinar on Acceptance Sampling Plans for Process Validation and Production Lot Monitoring

    Understand more about acceptance sampling plans for process validation and production lot acceptance by attending this audio conference. 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/Acceptance-Sampling-Plans-for-Process-Validation-and-Production-Lot-Monitoring-507734/JULY-2018-ES-TRAININGREGISTRY
  • 18 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
  • 19 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
  • 20 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