We issue food additive regulations specifying the conditions under which an additive has been demonstrated to be safe and, therefore, may be lawfully used. Any unapproved food additive used in a beverage or other conventional food causes the food to be adulterated under section 402(a)(2)(C) ...
内容提示: [Code of Federal Regulations] [Title 21, Volume 3] [Revised as of April 1, 2006] [CITE: 21CFR170] TITLE 21--FOOD AND DRUGSCHAPTER I--FOOD AND DRUG ADMINISTRATIONDEPARTMENT OF HEALTH AND HUMAN SERVICES SUBCHAPTER B--FOOD FOR HUMAN CONSUMPTION (CONTINUED) PART 170 FOOD ADDITIVES...
Objections and hearings relating to food additive regulations under section 409 (c), (d), or (h) of the Act shall be governed by part 12 of this chapter. [42 FR 14491, Mar. 15, 1977, as amended at 42 FR 15674, Mar. 22, 1977] Sec. 171.130 Procedure for amending and repealing ...
[Code of Federal Regulations] [Title 21, Volume 3] [Revised as of April 1, 2006] [CITE: 21CFR171] TITLE 21--FOOD AND DRUGS CHAPTER I--FOOD AND DRUG ADMINISTRATION DEPARTMENT OF HEALTH AND HUMAN SERVICES SUBCHAPTER B--FOOD FOR HUMAN CONSUMPTION (CONTINUED) PART 171 FOOD ADDITIVE PETITIONS...
FDA amends food additive regulationdoi:10.1016/0306-3747(87)90041-8NoneAdditives for Polymers
In recent months, one developing topic has captured the attention of manufacturers, the U.S. Food and Drug Administration (FDA), legislators, and consumer protection agencies—food additive regulations in the U.S. This article discusses the recent wave of state bills on food ...
Objections and hearings relating to food additive regulations under section 409 (c), (d), or (h) of the Act shall be governed by part 12 of this chapter. [42 FR 14491, Mar. 15, 1977, as amended at 42 FR 15674, Mar. 22, 1977] Sec. 171.130 Procedure for amending and repealing ...
8 When comparing your proposed use of a substance to existing animal food additive regulations, GRAS affirmation regulations, or GRAS conclusions in the inventory, bear in mind that a food additive regulation, GRAS affirmation, or GRAS conclusion is not for the substance itself, but for the ...
通用药物许可(Abbreviated New Drug Application, ANDA):适用于仿制药的上市许可申请。该许可要求提交对原始药物的生物等效性数据和其他相关资料。 食品添加剂许可(Food Additive Approval):适用于新的食品添加剂的许可申请。该许可要求提交对添加剂的安全性评估数据。 展开全文...
精选优质文档倾情为你奉上CodeofFederalRegulationsTitle21,Volume3RevisedasofApril1,2006CITE,21CFR171TITLE21FOODANDD