Differences in efficacy evaluation endpoints in clinical trials for claiming reduction of post-prandial glycemic response between Japan and the European Union-Reference-Cited by-同舟云学术

Differences in efficacy evaluation endpoints in clinical trials for claiming reduction of post-prandial glycemic response between Japan and the European Union

Published:2019-12-23 Issue:21 Volume:60 Page:3589-3593
ISSN:1040-8398
Container-title:Critical Reviews in Food Science and Nutrition
language:en
Short-container-title:Critical Reviews in Food Science and Nutrition

Author:

Tanemura Nanae¹^ORCID,Ito Keisuke¹,Hamadate Naobumi²,Koshizaka Masaya³,Urushihara Hisashi¹

Affiliation:

1. Division of Drug Development & Regulatory Science, Faculty of Pharmacy, Keio University, Tokyo, Japan;

2. Hamadate Science Office, Tokyo, Japan;

3. Division of Diabetes, Metabolism and Endocrinology, Chiba University Hospital, Chiba, Japan

Publisher

Informa UK Limited

Subject

Industrial and Manufacturing Engineering,General Medicine,Food Science

Link

https://www.tandfonline.com/doi/pdf/10.1080/10408398.2019.1700904

Reference26 articles.

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2. Consumer Affairs Agency. 2018a. FFC notification database. Accessed February 1, 2018. https://www.fld.caa.go.jp/caaks/cssc01/.

3. Consumer Affairs Agency. 2018b. FOSHU guideline. Accessed February 1, 2018. http://www.caa.go.jp/foods/pdf/syokuhin1567.pdf.

4. International legislation on nutrition and health claims

5. Implementation of the nutrition and health claim regulation – The case of antioxidants

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