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Food Labeling Q&A Reference Manual
Food Labeling Q&A Reference Manual "Thompson Publishing has long been a leader in producing food labeling resources. This new volume will be welcomed by those people who learn better with a question and answer style rather than a cataloging of facts."
 –Neal D. Fortin, Director of the Institute for Food Laws & Regulations and assistant professor  in the MSU College of Agriculture and Natural Resources

Find answers quickly to questions asked by real-world professionals


Thompson's brand new Food Labeling: Q&A Reference Manual includes questions asked by real-world professionals and answered by the FDA and top Food and Drug Law attorneys and consultants. Tackling issues related to all types of labeling questions, the Food Labeling: Q&A Reference Manual is a quick reference for all your labeling questions.
 

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Thompson's Food Labeling: Q&A Reference Manual is a quick reference guide for all your labeling questions.
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About This Publication
We know you have questions…who wouldn’t!  And you’re not alone other industry professionals have asked the same questions that are plaguing you!  In our new Q&A Reference Manual we tackle those questions for you.  We went to the FDA and top FDL attorneys for the answers so you’ll be able to have a clearer understanding of food labeling laws!
    
Example of some of the questions you’ll find covered….
•    What is required in the Nutrition Facts panel?
•    What heath claims can I legally make?
•    When can I use the term “light”?
•    How do I list the ingredients?
•    What does “serving size” mean?


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Audio Conferences

Tuesday, September 14 2010
A Drug Recall Case Study: Lessons Learned from a Widespread Drug Recall at a Major Pharmaceutical Company

Tuesday, September 21 2010
False Claims Act Liability for Pharmaceutical and Medical Device Companies: How Will Recent Changes Affect You?

Tuesday, September 28 2010
How Health Care Reform and Other New Legislation Will Affect the Regulation of Advertising and Promotion

Thursday, September 30 2010
FDA's Changes to the 510(k) Process: Are You Prepared?

Tuesday, October 05 2010
Device Complaint Handling: Implications for CAPA, Reporting, Recalls and More

Thursday, October 14 2010
Trial Master File: Ensure Your Trial Documentation Will Pass FDA Inspection


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