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Courses

  • 181 Request Info

    Webinar On New FDA FSMA Rules on the Sanitary Transportation of Human and Animal Foods

    If you are a shipper, carrier or receiver of foods not completely enclosed by a container or frozen, you have less than one year to establish a sound compliance system to fulfill the US FDA Law for the Sanitary and Temperature Controlled Transportation of Human and Animal Foods. The session will cover each section of the new sanitary food transportation law you need to protect consumers and your company.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-FDA-FSMA-RULES-SANITARY-TRANSPORTATION-501510/JUNE-2016-ES-TRAININGREGISTRY
  • 182 Request Info

    Webinar On Analytical Method Validation under Good Laboratory Practices (GLPs)

    This analytical method validation webinar will provide practical tips on how to validate an analytical method under the GLP requirements. It is recommended for laboratories that are under, or want to be under, Good Laboratory Practices (GLP) with FDA compliance training.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/GLPs-ANALYTICAL-METHOD-VALIDATION-501410/JUNE-2016-ES-TRAININGREGISTRY
  • 183 Request Info

    Webinar on FSMA Hazard Analysis and Risk-based Preventive Controls

    Overview: This session is focused on practical tools to help you design and implement HARPC. You will be able to develop a valid preventive control plan (PCP) from this session if you work with your associates to complete the step-by-step process to finalize the plan. We will also touch on the specific tools you need to document exactly what your people are doing to implement, maintain, validate, verify and continuously implement the plan through years to come. The training will take about 75 minutes and within a couple of hours after that, you will have a HARPC design that will be relatively easy to implement and use. Your fears and avoidance will be over once you learn how simple HARPC really is.
  • 184 Request Info

    Webinar on FDA NLEA Regulation for Retail and Foodservice Labeling - An Overview of Current Regulation and Pending Regulations

    The laws that regulate food labeling, especially under the NLEA, have been updated in recent years since the original regulations were written. There are also many pending changes that will affect regulation requirements. It is important to keep up with the changes to ensure compliance. 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-NLEA-REGULATIONS-501390/APRIL-2016-ES-TRAININGREGISTRY
  • 185 Request Info

    Seminar on New FDA FSMA Rules on the Sanitary Transportation of Human and Animal Foods

    Transportation and Logistics food transportation food safety rules are currently being finalized by the U.S. Food and Drug Administration (FDA). Under congressional instructions, the Food Safety Modernization Act (FSMA) requires the FDA to establish rules to improve, audit and enforce new food transportation rules. The rules provide a significant focus on foods not completely enclosed by a container, risk reducing adulteration prevention, personnel training and certification, inspection and data collection, maintenance and reporting that provides evidence of compliance. GlobalCompliancePanel Refer a Friend Program: Any Customer to 3 Referrals "Can Participate 2 Days Seminar for free of Cost
  • 186 Request Info

    Food Safety and Defense: Key Factors to Safely Manufacture, Package and Handle Food Products

    GlobalCompliancePanel Refer a Friend Program: Any Customer to 3 Referrals "Can Participate 2 Days Seminar for free of Cost This Seminar will focus on Food Defense and will detail what an organization needs to have in place in order to safely manufacture, package, and or handle food products. It will cover a broad range of: production types, facilities, and the transportation of goods. This webinar will highlight key areas of the organization that need to be controlled to ensure that intentional contaminants do not enter the product by potential threats.
  • 187 Request Info

    Preparing to Comply with the New FDA FSMA Rules: Planning Valid Preventive Food Safety Controls

    GlobalCompliancePanel Refer a Friend Program: Any Customer to 3 Referrals "Can Participate 2 Days Seminar for free of Cost Validation of preventive controls is where the rubber meets the road in terms of prevention. You can develop a food safety plan, implement the plan and verify the plan, but if your data does not prove that you are actually preventing food safety problems, the plan is not considered valid and your overall food safety effort will fail audits. According to the FDA all food facilities "must monitor their controls, conduct verification activities, provide hard data to validate that the controls are effective, take appropriate corrective actions, and maintain records documenting these actions". This training session will present a practical approach to provide you and your team members with needed understanding and tools and a basic strategy for designing, implementing and validating preventive process controls.
  • 188 Request Info

    Webinar on Optimizing Target Weights for Foods and Beverages

    This training program will elaborate factors affecting the target weight decision and help determine the tolerable risks of under-filling and the costs of over-filling. Attendees will gain an understanding of process stability and process capability concepts and methods for process optimization. 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/OPTIMIZING-TARGET-WEIGHTS-501306/APRIL-2016-ES-TRAININGREGISTRY
  • 189 Request Info

    Webinar on Combined HACCP Development & Risk- Based HACCP

    Developing an effective HACCP plan requires a clear understanding of the principles and specific steps involved in a HACCP study. This webinar will teach you through step by step process detailing how the user can build a plan capable of identifying and controlling food safety hazards relevant to your products and processes. Next, the user will be shown how to determine the significance of these hazards by applying risk assessment techniques, the output of which is a measure of risk which then allows you to put in place appropriate control measures. Finally, the session will breakdown much of the confusion and inherent weaknesses present in many food safety standards surrounding the determination of control measures in HACCP.
  • 190 Request Info

    Webinar on Food Safety - Food Certifications - What Certification is Best for Your Company?

    Since the Food Safety Modernization Act of 2010 became live in 2011 and the Global Food Safety Initiative (GFSI) began gaining significant ground since 2012, certification is now key to gain and maintain clients as well as ensure compliance. These requirements and mandates push every organization to ensure that they are up to date on their food safety programs. With the associated costs related to oversights and recalls, certification to food safety is an important economic aspect of any organization. This session is designed for food manufacturers, packagers and handlers and is focused towards helping both domestic and foreign entities in ensuring compliance with being secure and remaining compliant to pertinent regulations through gaining certification.
  • 191 Request Info

    Webinar on Ready- to-Eat Foods: Pathogens of Concern and Intervention Controls

    Consumer demand for minimally processed products with a longer shelf-life has resulted in the mass production and distribution of chilled convenience RTE foods. However, RTE foods remain a significant vehicle for foodborne pathogens such as Listeria monocytogenes. The challenges are enormous because production of RTE foods frequently involves extensive processing and packaging. Therefore, this webinar is designed to review current knowledge on the pathogens of concern, sources and intervention controls. The webinar will provide a review on the different RTE food types and pathogens of main concern. The sources of pathogens will be described along with cross-contamination points within the process.
  • 192 Request Info

    Webinar on Food Safety - Food Defense

    Since the Food Safety Modernization Act of 2010 was signed into law by President Obama on January 4, 2011, Food Defense is now clearly called out and must be adhered to. These requirements mandate FDA’s action in the area of Food Defense, and penalties continue to go higher and higher. With the associated costs related to oversights and recalls, Food Defense is an important economic aspect of any organization. This session is designed for food manufacturers, packagers and handlers and is focused towards helping both domestic and foreign entities in ensuring compliance with being secure and remaining compliant to FDA regulations.
  • 193 Request Info

    Webinar on FSMA Final Rules - Foreign Supplier Verification Program (FSVP) for Food Importers and Accredited Third-Party Certification

    This 60-minute webinar will offer an overview of the Foreign Supplier Verification Programs (FSVP) and the accredited third party certification rules identifying scope, key requirements and compliance dates or implementation dates. 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/FSMA-FINAL-RULES-501304/MARCH-2016-ES-TRAININGREGISTRY
  • 194 Request Info

    San Diego Conference on Food Safety and Defense: Key Factors to Safely Manufacture, Package and Handle Food Products

    This Seminar will focus on Food Defense and will detail what an organization needs to have in place in order to safely manufacture, package, and or handle food products. It will cover a broad range of: production types, facilities, and the transportation of goods. This webinar will highlight key areas of the organization that need to be controlled to ensure that intentional contaminants do not enter the product by potential threats.
  • 195 Request Info

    Phoenix Conference on Safe Production of Meat Products

    This seminar is designed for those that want to be involved with the production of safe meat products. Material to be discussed will provide participants knowledge of how sanitary practices can contribute to the production of safe meat products. Knowledge will be provided about contamination responsible for spoilage and foodborne illness and how hygienic practices can enhance the safety of meat products. Valuable knowledge will be provided about how to more effectively enhance hygiene and conduct effective sanitation practices during production and recommended procedures for efficient and effective cleaning. Also, participants will receive instruction about how to evaluate the effectiveness of a sanitation program.
  • 196 Request Info

    Conference on Preparing to Comply with the New FDA FSMA Rules: Planning Valid Preventive Food Safety Controls

    Validation of preventive controls is where the rubber meets the road in terms of prevention. You can develop a food safety plan, implement the plan and verify the plan, but if your data does not prove that you are actually preventing food safety problems, the plan is not considered valid and your overall food safety effort will fail audits. According to the FDA all food facilities "must monitor their controls, conduct verification activities, provide hard data to validate that the controls are effective, take appropriate corrective actions, and maintain records documenting these actions". This training session will present a practical approach to provide you and your team members with needed understanding and tools and a basic strategy for designing, implementing and validating preventive process controls. You will develop a basic plan during this training and have it checked by the instructor.
  • 197 Request Info

    Webinar onAerospace - AS9100 vs ISO 9001

    AS9100 was released in 1999, and was based on ISO 9001. As many different organizations wanted a standard for their industry, ISO 9001 did not cover all of the aspects needed to ensure safe materials and manufactured goods were acceptable for their aerospace applications. AS9100 takes the ISO 9001 requirements and supplements them with additional quality system requirements, which are established by the aerospace industry in order to satisfy DOD, NASA and FAA quality requirements. The intent of AS9100 is to establish a single quality management system for use within the aerospace industry.
  • 198 Request Info

    Webinar on FDA Regulations for Analytical Instrument Qualification and Validation Processes

    In this webinar you will learn the different global agencies expectations of analytical equipment qualification along with the development of a sound process validation program in order to develop and implement bulletproof solutions that are accepted, effective, and efficient. Through case study analysis we will examine best practices to provide thoughts and ideas to develop or improve the performance of your current system. Additionally, case studies will explore how your management practices of your analytical equipment qualification/ validation and process validation programs can help or hurt your legal liability and the legal issues that arise from nonconformance with regulators and Auditors.
  • 199 Request Info

    Webinar on Prepare Your Company to Meet the Final FSMA Subpart G Rule Requirements for the Receiver Liability for Supplier Preventive Controls

    Based on the FDA FSMA rules for preventive controls and their emphasis on planning for and implementing preventive systems, the final rules require that food supply chain members understand new supply-chain-applied control requirements. These requirements mean that food and food ingredient buyers must develop a system to collect appropriate supplier qualification and certification records as part of their approval of suppliers system. Generally, this data repository should be used to risk-rank suppliers for several reasons.
  • 200 Request Info

    Webinar on Laboratory-Developed Tests: Why does FDA think They Can Regulate Them, and Why Do Others Think They Cannot

    This presentation will review the legal definition of medical device, and how it is applied by FDA to in vitro diagnostic tests. It will review the history of FDA interest in LDTs, and will describe the current situation with respect to Laboratory-developed tests. It will describe tests which have been cleared by FDA and those which have attempted clearance but not been cleared. It will discuss possible future actions by FDA and by the US laboratory community and assess their probability.