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Courses

  • 101 Request Info

    Understanding the USP 1058 Analytical Instrument Qualification

    Overview: Analytical instruments should be qualified to demonstrate suitability for the intended use. Despite the fact that instrument qualification is nothing new and companies spend a lot of time, it is a frequently cited deviation in FDA inspectional observations and warning letters. Areas Covered in the Session: FDA and EU analytical instrument requirements Most common inspection problems Recommendations for firmware and software validation Roles and responsibilities: QA, manufacturer, user Qualification of existing systems
  • 102 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 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/SECRETS-WRITING-EXCELLENT-SOPs-504929/MARCH-2017-ES-TRAININGREGISTRY
  • 103 Request Info

    Webinar On Process Validation for Medical Device Compliance

    The FDA finds inadequacies in process validation with Medical Device firms frequently. In fact, the fourth most frequently-cited Form 483 observation for medical device firms is for Process Validation. Find out how you can avoid these observations and emerge from your FDA audit with zero observations! Medical device validation can be confusing, but this webinar will clear many of the misconceptions related to process validation for medical device companies and helps you to bring your validation program to ship-shape.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/MEDICAL-DEVICE-COMPLIANCE-502356/MARCH-2017-ES-TRAININGREGISTRY
  • 104 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 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/FDA-FTC-REGULATE-ADVERTISING-509777/MARCH-2017-ES-TRAININGREGISTRY
  • 105 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 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/DRUG-SUPPLY-CHAIN-SECURITY-ACT-DSCSA-502056/MARCH-2017-ES-TRAININGREGISTRY
  • 106 Request Info

    Webinar On Food safety- How to Prepare for Third party and Regulatory Audits

    This webinar will describe how to build a program for the preparation of a third party or regulatory audit. The webinar will describe what you should prepare for prior to an audit. This will include key programs such as sanitation, operations, pest control, preventative maintenance, allergens, HACCP and other key areas. The preparation will also include basic information on how both 3rd party and regulatory auditors conduct their inspections.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-SAFETY-504029/MARCH-2017-ES-TRAININGREGISTRY
  • 107 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 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/DATA-ANALYSIS-QSR-507590/FEBRUARY-2017-ES-TRAININGREGISTRY
  • 108 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 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/GMP-COMPLAINT-SYSTEMS-502049/FEBRUARY-2017-ES-TRAININGREGISTRY
  • 109 Request Info

    Food Microbiology Methods in Validation

    Overview: The Webinar will discuss the practical distinction between and method validation and method verification and the requirements of each analytical approach to comply with ISO/IEC Standard 17025:2005 for a microbiology laboratory accreditation. Areas Covered in the Session: The difference between method validation and verification The performance characteristics for method validation Performance requirements for method verification How to implement a verification protocol that defines a method’s fitness-for purpose Who Will Benefit: Quality Assurance Managers Laboratory Technicians Laboratory Managers Regulatory Compliance Officers Consultants New employees in your food safety and quality laboratories
  • 110 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 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/QUALITY-DESIGN-502012/FEBRUARY-2017-ES-TRAININGREGISTRY
  • 111 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 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/HUMAN-FACTORS-VALIDATION-ISO62366-FDA-502041/FEBRUARY-2017-ES-TRAININGREGISTRY
  • 112 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 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/DR-BCP-FDA-CYBER-ATTACKS-502020/JANUARY-2017-ES-TRAININGREGISTRY
  • 113 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 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/USP-797-USP-795-502001/JANUARY-2017-ES-TRAININGREGISTRY
  • 114 Request Info

    Webinar On Microsoft Excel Macros-4-Part Series: Your Key to Success In The Modern Business World

    The first part will provide you with a basic understanding of Excel macros. Program participants will learn how to automate repetitive tasks and learn more about Excel's Record Macro feature, discover how to store macros in a Personal Macro Workbook for future use and learn how to create a shortcut on the Quick Access Toolbar.Price:$800.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/MICROSOFT-EXCEL-MACROS-PART-4-502007/JANUARY-2017-ES-TRAININGREGISTRY
  • 115 Request Info

    Webinar On Microsoft Excel Series - Part 1: Shake Hands with Macros

    Part 1 of this four-part webinar series on Microsoft Excel macros will cover the automation possibilities that Excel macros offer and the nuances of Excel's Personal Macro Workbook. Excel expert David Ringstrom, CPA, will also define how to use Excel's Record Macro feature to automatize repetitive tasks, including cleaning up reports you've exported from an accounting package, creating your own keyboard shortcuts for Excel features and scrubbing your data. 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/MICROSOFT-EXCEL-SERIES-PART-1-502003/JANUARY-2017-ES-TRAININGREGISTRY
  • 116 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 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/SOP-ALLERGEN-CONTROL-PLAN-501982/JANUARY-2017-ES-TRAININGREGISTRY
  • 117 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 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/GOOD-POST-MARKET-SURVEILLANCE-501998/JANUARY-2017-ES-TRAININGREGISTRY
  • 118 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 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/MEXICO-FOOD-LABELING-502016/JANUARY-2017-ES-TRAININGREGISTRY
  • 119 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 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/FDA-FOOD-LABALING-CLAIMS-501924/DECEMBER-2016-ES-TRAININGREGISTRY
  • 120 Request Info

    Seminar on Validation, Verification and Transfer of Analytical Methods

    Analytical methods and procedures should be validated to ensure reliability, consistency and accuracy of analytical data. Compendial methods should be verified to demonstrate the suitability of laboratories to successfully run the method and when methods are transferred between laboratories successful transfer should be demonstrated through testing. In case a laboratory wants to use an alternative method instead of a compendial method, equivalency of the alternative method to the compendial method should be demonstrated. Method validation recently got highest attention from regulatory agencies and industry task forces. For example, FDA and EMA released guidelines on method validation and transfer, and USP has proposed new approaches chapters for integrated validation, verification and transfer of analytical procedures, for equivalency testing and for statistical evaluation.