Supplier Management

If you can't find what you want, Ask Us.

Refine Your Results

reset

Filter by Category

Location

Dates

FEATURED VENDORS

Showing 1-20 of 30 results Sort by:

Courses

  • 1 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
  • 2 Request Info

    Webinar on Mastering the Export Administration Regulations & 2018 Export Control Reform Changes

    Companies may find themselves subject to fines and penalties for violations of export regulations. The process of export compliance reform is ongoing. Make sure that your company is up to speed on the export regulations and how they impact your business operations. Designed for both novices and experienced exporters needing a refresher on EAR requirements, this webinar details the essential tools for mastering the EAR. Export Control Reform Act of 2018 (ECRA), seeks to modernize the U.S. dual use export control regime while addressing perceived threats to U.S. interests from non-U.S. competitors. 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/Mastering-the-Export-Administration-Regulations-2018-Export-Control-Reform-Changes-504075/SEPTEMBER-2018-ES-TRAININGREGISTRY
  • 3 Request Info

    FDA Recalls and Traceability Requirements through Food Processes

    Attend this webinar by John Ryan, you will go through traceability requirements and techniques useful during quality deviation investigations & potential FDA recalls. 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-Recalls-and-Traceability-Requirements-2018-Trends-and-Common-Issues-505974/JULY-2018-ES-TRAININGREGISTRY
  • 4 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
  • 5 Request Info

    Webinar on Cost Analysis in Purchasing

    Join webinar to know the difference between price and cost analysis, how to win in negotiations by understanding the elements of cost, and more. 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/Cost-Analysis-in-Purchasing-505252/JUNE-2018-ES-TRAININGREGISTRY
  • 6 Request Info

    Webinar on Bonified CAPA Investigations

    Attend this webinar to know how to conduct an effective investigation, identify root causes, and implement workable corrective action in a timely manner. 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/Bonified-CAPA-Investigations-503630/JUNE-2018-ES-TRAININGREGISTRY
  • 7 Request Info

    Webinar on Supplier Quality Metrics and Scorecards A Systems Approach

    Join this 90-minutes webinar that focus on establishing an effective and efficient system of purchasing controls that enables to provide safe products to the customers. 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/Supplier-Quality-Metrics-and-Scorecards-A-Systems-Approach-502730/MAY-2018-ES-TRAININGREGISTRY
  • 8 Request Info

    Webinar on CBP's First Sale Rule: Duty Saving Opportunity for Importers

    This webinar will help importers understand the First Sale Rule and whether their operations are ready to withstand a CBP review for this rule. 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/CBP-s-First-Sale-Rule-Duty-Saving-Opportunity-for-Importers-508081/MAY-2018-ES-TRAININGREGISTRY
  • 9 Request Info

    Webinar on Price Analysis and Total Cost of Ownership Concepts in Procurement

    This webinar discusses the fundamental to developing and implementing methods of Price Analysis and the concepts of Total Cost of Ownership. 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/Price-Analysis-and-Total-Cost-of-Ownership-Concepts-in-Procurement-505575/MAY-2018-ES-TRAININGREGISTRY
  • 10 Request Info

    Webinar on U.S. Customs Duty Drawback & Refunds Understanding the Recent Changes

    Learn how importers need to be aware about the new drawback regime and resulting refunds. 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/U-S-Customs-Duty-Drawback-Refunds-Understanding-the-Recent-Changes-505997/APRIL-2018-ES-TRAININGREGISTRY
  • 11 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:$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/Creating-a-Good-Design-History-File-DHF-for-Audit-Success-506030/MARCH-2018-ES-TRAININGREGISTRY
  • 12 Request Info

    Webinar on FDA - Streamlining Your Internal Auditing Process

    This webinar will cover creating of a value-added internal auditing program that is compliant to FDA cGMP/ Quality System Regulation and ISO 13485. It will include how to set up and manage the auditing system as well as how to conduct an internal audit and document the results and any nonconformities. It will discuss the value of a good internal auditing program. 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/FDA-Streamlining-Your-Internal-Auditing-Process-506001/MARCH-2018-ES-TRAININGREGISTRY
  • 13 Request Info

    Webinar on Step-by-Step Process for Successful Sterility Failure Investigations

    There is no one size fits all investigation for microbial contamination. Microbiological testing covers a wide range of products, processes and environments, therefore representative samples from each of these categories forms the basis of what gets investigated. The role of QC microbiology in the identification and investigation of various results from manufacturing areas and finished product testing is extremely important. When the need for an investigation arises, it is common for a cross functional team to convene involving all levels of management from various departments - quality control chemistry and microbiology, manufacturing, quality assurance, and, facilities and engineering.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/Step-by-Step-Process-for-Successful-Sterility-Failure-Investigations-506465/MARCH-2018-ES-TRAININGREGISTRY
  • 14 Request Info

    Webinar on Identifying and Managing the Hazards of Combustible Dust

    In order to ensure the safe operation of facilities handling combustible dust a balanced mix of engineering and administrative controls are required. This webinar will provide information on the safeguards used to mitigate the hazards associated with combustible dust and how to determine what is appropriate for your facility. 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/Identifying-and-Managing-the-Hazards-of-Combustible-Dust-503945/MARCH-2018-ES-TRAININGREGISTRY
  • 15 Request Info

    Webinar on Modeling and Optimizing Process/Product Behavior Using Design of Experiments

    Experimentation is frequently performed using trial and error approaches which are extremely inefficient and rarely lead to optimal solutions. Furthermore, when it's desired to understand the effect of multiple variables on an outcome (response), "one-factor-at-a-time" trials are often performed. Not only is this approach inefficient, it inhibits the ability to understand and model how multiple variables interact to jointly affect a response. 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/Modeling-and-Optimizing-Process-Product-Behavior-Using-Design-of-Experiments-503135/JANUARY-2018-ES-TRAININGREGISTRY
  • 16 Request Info

    Webinar on Spreadsheet Validation: Understanding and Satisfying FDA Requirements

    Many companies struggle with spreadsheet compliance. Some are still using invalidated spreadsheets. Many companies lack an understanding of how to satisfy FDA technical validation requirements as applied to spreadsheets. Most organizations lack a clear spreadsheet compliance strategy. An unplanned 'emergency' spreadsheet validation project could paralyze the organization. This webinar will describe methods for planning and executing spreadsheet validations that satisfy FDA 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/Spreadsheet-Validation-Understanding-and-Satisfying-FDA-Requirements-504170/JANUARY-2018-ES-TRAININGREGISTRY
  • 17 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
  • 18 Request Info

    Webinar on Effective Document Management in Regulated FDA Environments: A Primer for all Pharma, Biotech and Medical Device Companies

    To stay compliant, your organization must control all quality documentation, such as SOPs, policies, quality manuals, CAD files, and engineering change orders. However, many organizations find it difficult to manage these documents and prevent document changes from impacting other processes.Find out how to effectively and efficiently handle the cGMP/ISO document change control requirements in this webinar. You will understand how much information you need to document, what level of detail is required for compliance, and how to implement and maintain a sustainable change control system.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-Document-Management-in-Regulated-FDA-Environments-A-Primer-for-all-Pharma-Biotech-and-Medical-Device-Companies-506089/DECEMBER-2017-ES-TRAININGREGISTRY
  • 19 Request Info

    Webinar onEffective Pharmaceutical GMP Audits and Self-Inspections

    Regulators expect audits and self-inspections of the manufacturer to assure the quality of its own operations and those of its suppliers and contractors via repeated audits. FDA and other regulators have contributed to and endorsed ICH Q10, Pharmaceutical Quality System, which explicitly recommends audits as a key element in the review of process performance and product quality and also in the management of outsourced activities and purchased materials.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-Pharmaceutical-GMP-Audits-and-Self-Inspections-507109/DECEMBER-2017-ES-TRAININGREGISTRY
  • 20 Request Info

    Webinar on Purchasing Ethics: Doing What's Right Across All Supplier Interactions

    This topic will cover how you can make your procurements fair and open. How to provide an appearance that does not show favoritism. Discover internal controls you can establish to better regulate vendor interactions during a procurement activity. Tips will be provided on establishing office procedures that will avoid ethical conflicts. Attendees will come away with tools that they can implement to better avoid vendor protests and improve procurement documents at the same time. This topic will also cover how to defend against inappropriate vendor influences. 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/PURCHASING-ETHICS-DOING-WHAT-505124/NOVEMBER-2017-ES-TRAININGREGISTRY