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May 2013
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Food and Dietary Supplement Goods Manufacturing Practices

Online Event
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Overview

Course Description:

This webinar will provide perspective on how US food and dietary supplement companies should operate their manufacturing and holding facilities in compliance with FDA Good Manufacturing Practices (GMPs). It will also discuss the recent FDA enforcements trends, current issues and challenges to food industry in order to be compliant with the FDA GMP.

Course Objective:

In this highly-regulated arena, it is vitally important for food and dietary supplement companies to ensure that their products are made, packed and stored in full compliance with FDA Good Manufacturing Practices (GMPs).  This 90 minute session will help food and dietary supplement companies in the US understand the breadth and depth of good manufacturing practices that they can adopt into their manufacturing and holding operations. This webinar will discuss the following topics:

  • Statutory and regulatory history of Good Manufacturing Practices (GMPs)
  • Review of GMPs
    • Food GMPs in 21 CFR Part 110
    • Dietary Supplement GMPs in 21 CFR Part 111
    • Key differences between Food and Dietary Supplement GMPs
  • Implementation of GMPs
    • Which entities do they apply to?
    • Translation of GMPs into SOPs
  • Current trends and new developments
    • FDA enforcement activity
    • Key watch-outs
    • Food Safety Modernization Act
  • Related food safety standards 
    • HACCP and ISO 22000
  • Audit readiness
    • Ownership & accountability
    • Documentation

 

Who will Benefit:

This training on GMPs will provide valuable guidance to the following personnel in the food and dietary supplement companies:

  • Regulatory Affairs
  • Quality Assurance
  • Product Development
  • Product Supply
  • Laboratory operations
    • Analytical
    • Microbiology
  • Manufacturing  operations
      
    • Processing
    • Packaging
    • Distribution & holding operations
    • Legal
    • Internal Auditors
    • Risk Management

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