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  • 141 Request Info

    Webinar On Good Laboratory Practices (GLPs) - Comparing and Contrasting with Good Manufacturing Practices (GMPs)

    Attend the webinar to get a proper contrast and comparison of GMP and Good Laboratory Practices (GLPs), CFR part 58, for conducting nonclinical laboratory studies that support applications for research or marketing permits for products such as food and color additives, human and animal drugs, medical devices for human use, biological products and electronic products that are regulated by the FDA.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 142 Request Info

    Traceability and Recall Through Food Processes by Compliance4all

    Overview: This 60 minute webinar will cover traceability requirements and techniques useful in the event of quality deviation investigations and potential FDA Recalls. The session will also cover associated information like identification, classification and protocols. A variety of technologies at various price levels that are used for tracking and recall will be covered. There are quite a variety of potential applications ranging from simple case level bar code systems to more sophisticated satellite systems that include sensors for explosives, bacteria and other issues will be discussed. Test data from a number of these systems will be shown in cross country and trans-ocean applications. Farm, distribution center, blending operations, pallet level vs container and case level systems will be explored.
  • 143 Request Info

    Sanitizers for the Food Industry by Compliance4all

    Overview: Effective sanitation in the food industry involves the maintenance of clean conditions in the entire food operation. This status is attained through the destruction of residual microorganisms after cleaning of production, storage and service areas of food establishments. As food production, handling, and preparation techniques and eating habits change, food establishments remain a viable location for microbial proliferation. Microorganisms are viable sources for foodborne illness. The food establishment surroundings without effective preventive measures to retard microbial proliferation can attract pathogenic microorganisms that act as vectors of contamination and foodborne disease. As handling and modern processing methods increase the journey from production to consumption, the possibility of microbial contamination is increased. As contamination increases, the possibility of microorganisms that cause foodborne illness is increased.
  • 144 Request Info

    Control Food Safety and Quality by Compliance4all

    Overview: The course includes activities to help trainees develop a general plan and procedures to standardize and control food quality and safety transportation processes. For food shippers, carriers and receivers, standardization or upgrade to current practices is critical. For buyers, knowing how to establish standards for your food transporters sets the stage for required supply chain controls. The journey from "Where do we start?" to "We are compliant food safety carriers." begins here and establishes a basis for meeting newly evolving FSMA food safety during transportation requirements.
  • 145 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 Event link
  • 146 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 Event link
  • 147 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 Event link
  • 148 Request Info

    Webinar On Organic Labeling and Marketing - Changes in the Law and Certification Guidelines

    This training on Organic Labeling & Marketing will help the attendees understand the requirements of the USDA National Organic Program including the expectations in the agriculture sector. It will highlight the agricultural methods used to grow food and approved methods that integrate cultural, biological and mechanical practices.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 149 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 Event link
  • 150 Request Info

    Webinar On Medical Device CE Mark & Quality System Certification: Recent & Proposed Changes

    Medical devices sold into the European Union (EU) must comply with the applicable medical device directives, EU laws similar to FDA's regulations. Medical devices declared compliant must bear a CE mark in order to be admitted to the 28 member countries comprising the EU. The market population of these 28 countries is 450 million people, exceeding the 420 million people served by NAFTA (USA, Canada & Mexico), so many companies have an interest in penetrating this market.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 151 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 Event link
  • 152 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 Event link
  • 153 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 Event link
  • 154 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 Event link
  • 155 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: Event Link : Twitter Follow us – Facebook Like us –
  • 156 Request Info

    Webinar On Cosmetic Testing for US FDA Compliance

    The US Food and Drug Administration (FDA) holds cosmetic manufacturers and distributors responsible for the safety and quality of their cosmetics. This webinar serves to guide cosmetic manufacturers and distributors as well as other entities such as color additive manufacturers and analytical and microbiological laboratories on FDA recommendations and requirements concerning the safety and quality testing of cosmetics.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 157 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 Event link
  • 158 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 Event link
  • 159 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 Event link
  • 160 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 Event link