Food & Beverage - Operational Excellence/Quality

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  • 61 Request Info

    Webinar On Secrets for Writing Excellent SOPs (Standard Operating Procedures)

    Standard Operating Procedures (SOPs) are a critical ingredient in an effective and efficient Quality Management System. SOPs are typically one of the first things an investigator asks for in an inspection. Well written SOPs send a message to the FDA and Notified Bodies that your QMS is complete, accurate, and followed. More importantly, well written SOPs ensure that your personnel can consistently and accurately follow your processes resulting in correct outcomes and quality work. This webinar will help you structure your QMS and develop accurate, clear, unambiguous SOPs.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 62 Request Info

    Webinar On How the FDA & FTC Regulate Advertising & Promotion of Drugs & Dietary Supplements

    This webinar will cover FDA regulatory compliance requirements for all manufacturers and distributors who want to advertise and/or promote OTC drugs and dietary supplements in the U.S. The relationship between FDA and the FTC will be covered. Guidance will be provided on how to advertise OTC drugs and dietary supplements while avoiding misleading or unsubstantiated claims.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 63 Request Info

    Webinar On Three Years into the Drug Supply Chain Security Act (DSCSA): Where Does Industry Stand?

    The federal Drug Supply Chain Security Act (DSCSA) established new licensing, track-and-trace and preemption requirements for prescription pharmaceutical manufacturers, distributors and dispensers in the U.S. Three years have now passed since enactment of this law, but FDA has yet to publish key implementation standards. In the meantime, industry must comply with various deadlines. Individual state agencies also continue to act to fill perceived voids, complicating efforts toward national uniformity for operations.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 64 Request Info

    Webinar On Data Analysis in QSR

    Data analysis is one of the most powerful improvement tools because it can lead to cost reductions and preventive action. To use these techniques you need to know both the regulatory requirements and the analysis framework. This presentation provides that essential information.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 65 Request Info

    Webinar On GMP Complaint Systems, Adverse Event Reporting and Product Recalls

    This training program will provide the regulatory requirements for complaint handling in the pharmaceutical industries. The course will touch on complaint sources and details will be furnished on the interrelationships regarding complaint handling and product recalls. The course will also include timeline requirements associated with adverse event reporting.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 66 Request Info

    Webinar On Quality by Design

    This webinar will help you learn the basics of design controls for medical devices. This webinar will focus on the fundamental concept that quality cannot be inspected in--it must be designed in. We'll cover the regulations and expectations for design control. We'll discuss how design control fits into your Quality Management System. Successful integration can enhance your new product development process.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 67 Request Info

    Webinar On How to Conduct a Human Factors Validation Test Following ISO62366 and the FDA Guidance

    Validation testing aims to show that a device can be used by the intended users without serious use errors or problems, for the intended uses and under the expected use conditions. This webinar will explain the procedure described in ISO62366 and the 2016 FDA Guidance for a compliant human factors/ usability validation test. HF/U validation is very different from device validation.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 68 Request Info

    Webinar On Disaster Recovery (DR) and Business Continuity Planning (BCP) Best Practices for an FDA-Regulated Environment Increasingly Challenged by Cy

    This course is intended to provide specific guidelines for coaching attendees on the best practices for Disaster Recovery (DR) of computer systems and data and for Business Continuity Planning (BCP), including the handling of documentation in the event operations are disrupted. We will discuss the various types of risks, including cyber threats, power outages and others that could render an organization paralyzed in the absence of good planning.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 69 Request Info

    Webinar On USP 797/USP 795: Reviewing the Proposed Changes & How to Create and Manage a State of Control in Pharmacies

    USP standards serve as a professional guide for compounding practices and medication administration. USP standard 797 will be finalized in February 2018 and will be used for survey purposes. USP standard 800, which was finalized in February 2016, is focused entirely on employee safety when handling hazardous medications.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 70 Request Info

    Webinar On SOP for Allergen Control Plan

    This webinar will describe how to create an Allergen SOP to control all potentially hazardous allergens used in production of food. During the course of the webinar we will detail 8 major allergens, proper receipt and storage for allergens, handling of allergens, separation required for each allergen type and non-allergens, equipment needed, labeling procedure needed, allergen testing and lab resource for testing, recalls that have been necessitated due to allergens, cleaning procedures for allergens, production planning for when running allergen products.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 71 Request Info

    Webinar On Good Post-Market Surveillance

    Post-Marketing Surveillance (PMS) is the practice of monitoring the safety of a pharmaceutical drug or medical device after it has been released on the market and is an important part of the science of pharmacovigilance. The purpose of post-market surveillance is to protect individual health and public health through continued surveillance of products once they are placed on the market by reducing any risks.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 72 Request Info

    Webinar On Complying with Mexico Food Labeling Requirements: Retail & Private Label Opportunities in Mexico

    All importers and producers of processed food products must be aware of the new regulations and apply it in their labels for final consumer. Attend the webinar to know and understand the Mexican labeling standard as well as and the new requirements regarding the use of Front of Pack icons and the voluntary request of a nutritional Logo. The speaker will also explain the steps to follow in order to gain an 'organic' status.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 73 Request Info

    Webinar On FDA Food Labeling Claims - Understanding the Advantages and the Risks of Claims

    Join this conference by expert speaker Natasha Rowley-Phipps to review the types of food labeling claims with an in-depth review of the regulations. Get insights on claims in the market place with examples and review of case studies of claims with enforcement actions taken by the FDA.This session will help both regulatory and marketing departments navigate this complex area of regulations while taking maximum business advantage of these regulations.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 74 Request Info

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

    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. In this two day workshop conference you will learn the legal requirements, how to develop a company plan that meets FDA and your customer requirements. You will review and learn how to establish appropriate temperature monitoring, sanitation, container test and traceability, training and data reporting procedures.
  • 75 Request Info

    Webinar On Judicial Imperative for Mitigating Recalls and Outbreaks in Food Industry

    Food industry experts in risk management, compliance, quality assurance, and regulatory affairs all share in the responsibility to ensure that their company complies with state and federal laws. This course focuses on key federal regulations and Congressional Acts behind some of the most notable prosecutions and fines in the industry. Further, decisions by U.S. District and Supreme Court Justices have played a significant role in the changing prosecutorial landscape for the food industry.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 76 Request Info

    Webinar On Food Safety Modernization - Food Importer/VQIP Program

    This 75-minute webinar will offer an overview of the Foreign Supplier Verification Programs (FSVP) that will come into effect May 2017. Scope, key provisions and compliance dates will be discussed. The talk will focus on the risk-based activities that qualified individuals will need to implement in order to comply with FSVP regulatory requirements. Exemptions and modified requirements will be presented.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 77 Request Info

    Webinar On Application of CMS Quality Indicator Process in Healthcare Food Service

    The Centers for Medicare & Medicaid Services (CMS), in collaboration with public and private partners, is transforming how they conduct business and operations, connect providers and empower consumers and their beneficiaries.CMS enhances its partnerships in a delivery system where providers are supported in achieving better outcomes in health and health care at lower cost for the beneficiaries and communities they serve.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 78 Request Info

    Webinar On Food Defense - FSMA's New Intentional Adulteration Rule and How to Build your Food Defense Plan to Comply

    All of the most recent regulations required for food manufacturers can leave regulatory departments swimming in new programs to write or amendments to be made to current programs. Beyond ensuring that your programs are written and followed properly there are training requirements that must be met. Attendees will leave with knowledge of the final rule requirements related to food defense under the Food Safety Modernization Act.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 79 Request Info

    Webinar On FDA Action on Antiseptic Wash Products: What is Next for the Industry?

    The FDA just banned 19 active ingredients that are used in antibacterial soaps. This major regulation will have a huge impact on this multi-million-dollar industry since the FDA Rule will require companies to remove these ingredients from their products or remove the products from the market. Manufacturers will have one year to take these products off the market or reformulate them.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 80 Request Info

    Webinar On Understanding the Mexican Standard NOM-086-SSA1-1994 for food and beverages with modifications in its composition

    In this 90 minutes session, attendees will learn the Mexican standard about food and non alcoholic beverages with modifications on its composition and nutrimental specifications.This standard was created in order to attend the relationship between health and nourishment combined with the existence of numerous food products modified on its composition because of the elimination or the addition of nutriment, that's why it was necessary to establish nutrimental specifications in order to give correct information to the Consumer.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link