Medical Foods: Science, Regulation, and Practical Aspects. Summary of a Workshop

Author:

Holmes Jennifer L1ORCID,Biella Alexandre2,Morck Timothy3,Rostorfer Jena4,Schneeman Barbara5

Affiliation:

1. Medical Editing Services, Wichita Falls, TX, USA

2. Regulatory Affairs US, Nestlé Health Science, Bridgewater, NJ, USA

3. Spectrum Nutrition, LLC, Oxon Hill, MD, USA

4. Regulatory Affairs, Abbott Laboratories, Columbus, OH, USA

5. Department of Nutrition, University of California, Davis, Davis, CA, USA

Abstract

ABSTRACT On August 13–14, 2019, the Healthcare Nutrition Council and the ASN held the Medical Foods Workshop: Science, Regulation, and Practical Aspects. Medical food products help patients manage their disease and improve their quality of life. Yet many hurdles exist to getting patients new products. In this workshop, participants addressed some of these hurdles, with specific emphasis on topics like the statutory term distinctive nutritional requirements, the regulatory term modification of the diet alone, the role of clinical guidelines, the requirement that medical foods be used under medical supervision, and differentiation of foods for special dietary use from medical foods, as well as product innovation and future research. Real-world examples were discussed for intractable epilepsy, diabetes, end-stage renal disease, and inflammatory bowel disease.

Funder

HNC

Publisher

Oxford University Press (OUP)

Subject

Nutrition and Dietetics,Food Science,Medicine (miscellaneous)

Reference78 articles.

1. 21 CFR Ch. I. [Docket No. 96N–0364] RIN 0905–AD91. Regulation of Medical Foods. Advance notice of proposed rulemaking;Department of Health and Human Services, Food and Drug Administration;Fed Regist,1996

2. 21 CFR Chapter 1. [Docket No. 2002N–0434] Withdrawal of certain proposed rules and other proposed actions;Department of Health and Human Services, Food and Drug Administration;Fed Regist,2004

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