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Courses

  • 81 Request Info

    Webinar On Guidelines for F-Tag (F371) Food Sanitary Conditions Healthcare Setting

    Healthcare Managers Annual Review; CMS Guidelines for Food Sanitary Condition in healthcare settings. With regard to the revised guidelines for investigative protocols for F-Tag (F371) Sanitary Conditions, there have been significant changes in not just methodology of determining safe food handing but CMS has stepped up educating of survey team on interpretation of regulations by regulators.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/FOOD-SANITARY-CONDITIONS-HEALTHCARE-501845/NOVEMBER-2016-ES-TRAININGREGISTRY
  • 82 Request Info

    Webinar On Overview of the Mexican Labeling Standards and the New Labeling Requirements

    In this 90 minutes session, attendees will learn the Mexican labeling standard as well as and the new requirements regarding the use of Front of Pack icons and the voluntary nutritional quality seal. The regulation has been amended; the most significant change with the new regulations is the mandate to include an FOP nutrition label with information icons on saturated fat, other fat, sugar, sodium, and energy as a percentage of daily nutrients. 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/NEW-MEXICAN-LABELING-REGUIREMENTS-501822/NOVEMBER-2016-ES-TRAININGREGISTRY
  • 83 Request Info

    Webinar On Key Success Factors to reduce your risk of FDA Citations

    Does your company have the symptoms of a sick Quality System? This webinar will help you recognize the symptoms. You will learn about the risks and what you can do about them. Learn from an industry expert how you can improve your Quality Management System.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/RISK-FDA-CITATIONS-501812/OCTOBER-2016-ES-TRAININGREGISTRY
  • 84 Request Info

    Webinar On Mandatory GMO Labeling: Preparing for Implementation

    Public and scientific opinion on GMOs in the US is controversial and GMO labeling requirements have been a subject of much debate in the country. One of the U.S. states just enacted a GMO labeling law and a new Federal GMO Labeling law was passed in July 2016. Attend this webinar to learn about the status of GMOs in the U.S., how they are regulated by the FDA, FDA's Biotechnology Policy and Biotechnology Consultation program and GMO labeling in other countries.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/GENETICALLY-MODIFIED-ORGANISMS-USA-501772/OCTOBER-2016-ES-TRAININGREGISTRY
  • 85 Request Info

    Webinar On Laboratory Instrument Calibration: Current FDA Regulatory Requirements and Best Practices

    This web seminar builds on the terminology found in 21CFR160 (b)(4) and introduces terminology and concepts not found in the regulation, but necessary for an effective calibration program, such as instrument classifications. It applies measurement uncertainty or test accuracy ratio to specific calibration procedures and the selection of standards to provide scientifically sound calibrations traceable to national references.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/LABORATORY-INSTRUMENT-CALIBRATION-501728/OCTOBER-2016-ES-TRAININGREGISTRY
  • 86 Request Info

    Webinar On Adverse Event Reporting - Best Practices Dietary Supplements

    Adverse Event Reports should be a major concern for dietary supplement companies as adverse events can happen at any time. Adverse Event Report issues can be overwhelming for any business, but with the right system in place, there's no need to fear. Reporting and documenting serious adverse events in a timely manner for the Food and Drug Administration (FDA) is a necessity for the dietary supplement industry.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/DIETARY-SUPPLEMENTS-501765/OCTOBER-2016-ES-TRAININGREGISTRY
  • 87 Request Info

    Webinar On Substantiation of Food and Supplements Marketing Claims: FDA and FTC Requirements

    This webinar gives a clear overview of claims about food products and supplements in labeling, advertising and other forms of promotion. The material will be presented in layman's terms, so it can be understood by business and marketing executives who have no legal background. The webinar will include examples and will cover different types of products and product claims; labeling, advertising and social media, the roles of various government agencies, using testimonials, and sources of additional information.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/FDA-FTC-REQUIREMENTS-501745/OCTOBER-2016-ES-TRAININGREGISTRY
  • 88 Request Info

    Webinar On FDA Vs Health Canada

    This training program will demonstrate the similarities and differences between the FDA and Health Canada GMPs that regulate the manufacturing of pharmaceutical products. The course will also offer a review of the background and history behind the FDA and Health Canada. This training will review the requirements for both the FDA and Health Canada so that the observer will understand how to comply with both sets of laws.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/FDA-HEALTH-CANADA-501770/OCTOBER-2016-ES-TRAININGREGISTRY
  • 89 Request Info

    Webinar On Pharmaceutical and Biologics Facility Design: FDA and Regulatory Aspects

    This webinar will cover what is important in facility design from the FDA and regulatory standpoint. You will understand what FDA looks for during a facility inspection. You will be able to minimize possible design errors which are difficult and expensive to fix post-build. Understand what FDA looks for in reviewing the facility design and the flow patterns.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/PHARMACEUTICAL-BIOLOGICS-DESIGN-501777/OCTOBER-2016-ES-TRAININGREGISTRY
  • 90 Request Info

    Webinar On FDA's Two New Draft Guidance on Software and Device Changes and the 510(k)

    This course is intended to provide an overview of 2 new FDA draft guidance documents that clarify when medical device and software manufacturers must file a 510(k) (premarket notification) for changes to an existing device and/or software integrated with a device.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/FDAs-SOFTWARE-DEVICE-510k-501790/OCTOBER-2016-ES-TRAININGREGISTRY
  • 91 Request Info

    Webinar on October 2016 Clinical Trials Program

    Overview: The topic is device clinical trials. This term refers to the use of medical products on/in humans, in order to gain useful knowledge about the product. Such knowledge might be required to enable the development of user instructions, better understanding of limitations, evidence of clinical usefulness, or elements of product design that require additional changes. Who Will Benefit: R&D and Regulatory Staff Management of R&D Regulatory Contact Detail: Compliance4All DBA NetZealous, Phone: +1-800-447-9407 Email: support@compliance4All.com http://www.compliance4all.com/ Event Link : http://bit.ly/2aWhBD3 Twitter Follow us – https://twitter.com/compliance4all Facebook Like us – https://www.facebook.com/Compliance4all
  • 92 Request Info

    Webinar On Understanding Proper Labeling & Packaging Requirements & How to Stay Legally Compliant

    This course will cover labeling and packaging requirements. Every product created for consumption needs to be properly labeled to ensure transparency of not only the contents inside, where they came from, but also how to handle them for optimum quality. The discussion will be categorized by several types of product categories, as well as the various standards.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/LABELING-PACKAGING-LEGALLY-COMPLIANT-501689/OCTOBER-2016-ES-TRAININGREGISTRY
  • 93 Request Info

    Webinar On FDA's Update on Elemental Impurities According to the new ICH Q3D and USP 232/233 Guidelines - Are you ready?

    New, dramatically different requirements for elemental impurities will soon be introduced for most pharmaceutical products. These requirements cover more metals and require lower limits than the antiquated Heavy Metals test.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/FDAs-UPDATE-NEW-ICH-Q3D-USP-232-233-501732/SEPTEMBER-2016-ES-TRAININGREGISTRY
  • 94 Request Info

    Webinar On FDA Regulations for Marketing Dietary Supplements in the U.S

    In order to successfully market dietary supplements in the United States, it is essential to understand FDA's dietary supplement regulations and trends. This webinar will offer an excellent overview of FDA requirements for marketing, labeling, and promotion of dietary supplements in the U.S. The speaker will cover how dietary supplements can be effectively marketed in compliance with FDA requirements as well as structure/function claims, and their importance to supplement compliance in general.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/FDA-MARKETING-DIETARY-US-501704/SEPTEMBER-2016-ES-TRAININGREGISTRY
  • 95 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
  • 96 Request Info

    Webinar On Setting and Measuring Quality Objectives

    The Quality Objectives, derived from the Quality Policy, must be measurable. Good metrics have characteristics that make them clear and understandable. This presentation describes three types of metrics, illustrates how to use them for the Quality Objectives, and provides examples developed using Excel. One of the metric types, related to cycle time, has a particularly interesting graph type available in Excel.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/SETTING-MEASURING-QUALITY-OBJECTIVES-501634/SEPTEMBER-2016-ES-TRAININGREGISTRY
  • 97 Request Info

    Webinar On Legal, Regulatory and Policy Issues Related to Computer System Validation as the FDA Regulates Tobacco Products

    Effective and compliant computer system validation is critical to any FDA-regulated organization, including those manufacturing, testing and distributing tobacco products. During the past 30 years, best practices have been developed for other FDA-regulated industries to ensure that the cost of building and managing a computer system validation program for this purpose, along with the necessary policies and procedures.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/LEGAL-REGULATORY-POLICY-VALIDATION-FDA-501540/SEPTEMBER-2016-ES-TRAININGREGISTRY
  • 98 Request Info

    Webinar On FDA's Pet Food Labeling Guidelines

    This webinar will discuss the legal requirements for labeling pet or animal food. It will cover aspects of labeling such as the product name, the guaranteed analysis, the nutritional adequacy statement, feeding directions and calorie statements.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/FDAs-PET-FOOD-LABELING-501705/SEPTEMBER-2016-ES-TRAININGREGISTRY
  • 99 Request Info

    Webinar On How to prepare for and Host FDA Inspection and Avoid 483's

    In this webinar you will learn about the types of FDA inspections, necessary preparations such as assigning dedicated personnel to specific tasks for the inspection, facility requirements to support the inspection, the value of mock audits, how company personnel should conduct themselves during the inspection, how the inspection will unfold and how to respond to 483's.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/HOST-FDA-INSPECTION-AVOID-483s-501677/SEPTEMBER-2016-ES-TRAININGREGISTRY
  • 100 Request Info

    Webinar On Trial Master File (TMF): FDA Expectations from Sponsors and Sites

    This webinar will help participants learn what is required of a Trial Master File for a clinical trial, and will acquire a practical understanding of how these documents provide evidence for the regulated activities of the investigator and the sponsor. Also, Attendees will learn which documents are essential, and which ones are not necessary in the event of an FDA audit.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/TRIAL-MASTER-FILE-FDA-EXPECTATIONS-SPONSORS-SITES-501613/AUGUST-2016-ES-TRAININGREGISTRY