Food & Beverage

If you can't find what you want, Ask Us.

Refine Your Results

reset

Filter by Category

Location

Dates

FEATURED VENDORS

Showing 81-100 of 228 results Sort by:

Courses

  • 81 Request Info

    Webinar On Medical Device Reporting Requirements for Manufacturers Final Guidance

    This webinar explains the MDR regulation considering the new information contained in the Guidance and describes a compliant MDR procedure. Areas covered will include death, injury and mal-function reporting requirements, record keeping requirements, report timing, clarification of the term ‘becoming aware’ and clarification of reporting using electronic form 3500A.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-MDR-REGULATION-506828/MAY-2017-ES-TRAININGREGISTRY
  • 82 Request Info

    Webinar On Test Method Validation to Verify your Device Performance

    This webinar will help you have an understanding of Test Method Validations to verify the performance of a Medical Device, global reference standards, the FDA requirements and how to perform successful TMV to ensure your inspection of verification is effective, using detailed real-life case studies.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/TEST-METHOD-MEDICAL-DEVICE-508490/MAY-2017-ES-TRAININGREGISTRY
  • 83 Request Info

    Webinar On Failure Mode and Effect Analysis (FMEA) – Risk Analysis and Management

    Failure Mode and Effects Analysis (FMEA) is a systematic method for preventing failure through the discovery and mitigation of potential failure modes and their cause mechanisms. Actions are developed in a team environment and address each high: severity, occurrence or detection ranking indicated by the analysis. Completed FMEA actions result in improved product performance, reduced warranty and increased product quality.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/FMEA-RISK-ANALYSIS-MANAGEMENT-508377/APRIL-2017-ES-TRAININGREGISTRY
  • 84 Request Info

    Webinar On Regulatory Challenges Facing In-Vitro Diagnostic in U.S.

    In-vitro diagnostic (IVD) products drive a significant portion of clinical decision making today. IVDs assist in the identification, diagnosis and monitoring of disease. They play an ever-expanding role in the selection of appropriate therapeutic interventions in healthcare delivery with the advent of personalized medicine. These key products are a distinct class of medical devices regulated in the US by the Food and Drug Administration (FDA).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/REGULATORY-CHALLENGES-VITRO-DIAGNOSTIC-US-508213/APRIL-2017-ES-TRAININGREGISTRY
  • 85 Request Info

    Webinar On Best Practices for Preparation for, Behavior during, and Response to an FDA Inspection

    This is a detailed course designed to provide medical device/pharmaceutical professionals with the information they require to prepare for and manage FDA inspections. This course provides the rationale, strategies and flow on how to plan for an inspection, the inspection process and approach, and which company roles should be assigned for these types of inspections, among other related topics.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/RESPONSE-FDA-INSPECTION-508464/APRIL-2017-ES-TRAININGREGISTRY
  • 86 Request Info

    Webinar On Effective Purchasing and Supplier Controls for Medical Device Manufacturers

    This webinar can help you understand your responsibilities in terms of Purchasing Controls enabling you to provide safe and effective products to your customers. Learn how to prevent quality and compliance problems by having a strong system for Purchasing Controls! This webinar will help you to understand the regulations and how you can translate them into an efficient and effective process for purchasing/ supplier control.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/PURCHASING-SUPPLIER-CONTROLS-505726/APRIL-2017-ES-TRAININGREGISTRY
  • 87 Request Info

    Webinar On Understanding Corrections and CA&PA;

    This presentation explains the differences as well the QMS requirements to help you understand, implement, and maintain the effective systems.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/UNDERSTANDING-CORRECTIONS-CA-PA-509049/APRIL-2017-ES-TRAININGREGISTRY
  • 88 Request Info

    Webinar On FDA to Redefine 'Healthy Claim' for Food Labelling

    In order to make a 'Healthy' claim for Food Labeling and promotion, it's important to understand how FDA defines and will likely redefine the 'Healthy' claim. 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-HEALTHY-CLAIM-502129/APRIL-2017-ES-TRAININGREGISTRY#
  • 89 Request Info

    Webinar On CMO Supplier Quality Agreements - How to Comply with New FDA and EU Guidelines for Contract Drug Manufacturing

    This Webinar presentation will provide a thorough understanding of the content that is expected in Quality Agreements from a regulatory perspective. 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/CMO-SUPPLIER-QUALITY-AGREEMENTS-503052/APRIL-2017-ES-TRAININGREGISTRY#
  • 90 Request Info

    Webinar On Medical Device Premarket and Post market Cyber security following the new FDA Guidances

    Medical devices, like other computer systems, can be vulnerable to security breaches, potentially impacting the safety and effectiveness of the device. This vulnerability increases as medical devices are increasingly connected to the Internet, hospital networks and to other medical devices. This webinar will describe a program that will minimize risk to the user from cyber attacks.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-PREMARKET-509863/APRIL-2017-ES-TRAININGREGISTRY
  • 91 Request Info

    Webinar On Preparing a US FDA Medical Device 510(k) Submission and Deciding When to Submit a 510(k) for a Change to an Existing Device

    This webinar ensures your company gets a broader perspective of how and what to do to get a quick and non-debatable or questionable approval for your 510K product. All are different so this presentation will not just be specific for a specified Medical Device that is currently being marketed and your company wants the same opportunity to produce and sell that product.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/US-FDA-MEDICAL-DEVICE-510k-508586/APRIL-2017-ES-TRAININGREGISTRY
  • 92 Request Info

    Webinar On New GS1 US Guideline - Pharmaceutical Industry Prepares for DSCSA Item-Level Traceability Requirements

    New provisions of the 2013 Drug Supply Chain Security Act (DSCSA) will come into effect in 2023. The industry is using the newly updated GS1 Guideline to update their systems to comply with the law. There are many new features in the guideline that need to be understood before making changes to existing systems. 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/NEW-GS1-US-GUIDELINE-506697/APRIL-2017-ES-TRAININGREGISTRY
  • 93 Request Info

    Webinar On Falsifying Data in Clinical Trials: What to Report?

    Falsifying data in clinical trials is also considered data fraud. When data fraud occurs there are most likely other unreported or undetected misconduct that occurred within a clinical trial. This leads to poor, unreplicable results. When results cannot be replicated, questions arise about why a trial was conducted and what types of risks or harms were the participants exposed to.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/FALSIFYING-DATA-CLINICAL-TRIALS-502132/MARCH-2017-ES-TRAININGREGISTRY
  • 94 Request Info

    Webinar On How to Buy COTS Software, Audit Vendors and Validate the Software

    This presentation will focus on instructing attendees on best practices for buying COTS (Commercial Off-The-Shelf) software and evaluating software vendor(s). Presentation will highlight essential data and systems subject to Part 11 & Annex 11 (ERES - Electronic Records and Electronic Signatures) compliance while listing requirements for IT infrastructure, Laboratories, Manufacturing/ Operations, R&D, Regulatory and other GxP relevant areas of an FDA regulated manufacturer. 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/COTS-SOFTWARE-AUDIT-VENDORS-505707/MARCH-2017-ES-TRAININGREGISTRY
  • 95 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/MARCH-2017-ES-TRAININGREGISTRY
  • 96 Request Info

    Webinar On Classifying Medical Devices - US and EU

    This webinar will detail the medical device classification process for the United States through the FDA and will overview the very complex process for medical device classification within the EU. Specifically, this webinar will provide detailed background into the process and will make clear some of the very complex terms and sub-processes associated with medical device classification. We will actually work through the classification process step-by-step for the US and will overview how the process is accomplished for the EU.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/CLASSIFYING-MEDICAL-DEVICES-505796/MARCH-2017-ES-TRAININGREGISTRY
  • 97 Request Info

    Webinar On Quality Systems Inspection Technique (QSIT) and How to use it to Your Advantage

    Can your organization survive a Food and Drug Administration (FDA) inspection? Are you aware of the different aspects of your business that the FDA will be inspecting? This course, "FDA's Quality System Inspection Technique (QSIT)," is intended to facilitate manufacturer compliance with the FDA's Quality System Regulation (QSR) and related regulations, and increase inspection consistency, product quality, and the efficiency of the enforcement action review 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-SYSTEMS-INSPECTION-TECHNIQUE-505266/MARCH-2017-ES-TRAININGREGISTRY
  • 98 Request Info

    Webinar On The new Food Concern Spectrum: Food Authenticity

    While the concerns over food fraud trend after notable events, this webinar steps up into a higher elevation approach to the issue. Food Fraud is one of five key areas of food concerns under the umbrella of food authenticity. The list of concerns includes: Food Quality, Food Safety, Food Fraud, Food Defense, and Food Security. This course will help attendees understand the specific risks for each of the five concerns and how they are different from each other.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-AUTHENTICITY-502280/MARCH-2017-ES-TRAININGREGISTRY
  • 99 Request Info

    Webinar On How to Apply for a Breakthrough Therapy Designation and Win It

    This webinar, presented by a leading regulatory affairs expert with successful BTDs, discusses FDA expectations from BTD requests, the best practices to write a BTD request, and pros and cons of applying for a BTD. The session will highlight key regulatory requirements, dos and don'ts, common areas of concern, and trouble-shooting BTD requests using case studies and examples from the presenter's vast experience helping companies big and small in successfully applying for a BTD.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/BREAKTHROUGH-THERAPY-DESIGNATION-504525/MARCH-2017-ES-TRAININGREGISTRY
  • 100 Request Info

    FDA Regulations for instrument Qualification and Validation Processes

    Overview: 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. Why Should You Attend: The cost of non-compliance is therefore more than that of compliance. Are you in compliance with the FDA regulations for analytical equipment qualification and validation in your facility?