Skip to main content

Currently Skimming:

4 Performance Specifications
Pages 129-140

The Chapter Skim interface presents what we've algorithmically identified as the most significant single chunk of text within every page in the chapter.
Select key terms on the right to highlight them within pages of the chapter.


From page 129...
... The EFP will be consumed under worldwide environmental extremes. It is essential that this item be produced in accordance with Good Manufacturing Practices applicable to ready-to-eat food products.
From page 130...
... . Odor and Flavor The EFP shall be slightly sweet with blended cereal flavor from the base ingredients, and no distinct flavor notes attributable to the protein source or vitamin and mineral additions may be present.
From page 131...
... . Acceptability A prototype of the finished product shall be tested by the procuring agency and must receive a hedonic score of 6.0 or better on a 1.0- to 9.0-point scale, where 9.0 represents "like extremely" when assessed by likely target populations under conditions simulating field use (e.g., during 3 to 7 days' consumption)
From page 132...
... Glucose 2 g Lactose 4 g Monosaccharides 5.8 g Sodium 0.30 g 0.33 g Potassium 0.40 g 0.47 g Chloride 0.47 g 0.51 g Calcium 180 mg 207 mg Phosphorus 172 mg 206 mg Magnesium 44 mg 54 mg Chromium 3.0 log Copper 131 log 156 fig Iodine 24.5 log 53.6 fig Minimum Required Nutrient Density/l,OOO kcal 39g (35% of calories) 34g (13.5% of calories)
From page 133...
... (25% of calories) use of sugar or high fructose corn syrup 18 g 6 gig of Na; from malto dextrins 17 g 36 g Should be present only if milk solids are used 25 g 53 g < 25% by weight of car bohydrates 1.4 g 2.7 g 3.0 g EFP should not taste salty 2.0 g 3.5 g 4.2 g EFP should not taste bitter 2.2 g 4.2 g 4.6 g Equimolar to sodium 885 mg 1,620 mg 1,865 mg Phosphate, citrate, or carbonate salt forms 890 mg 1,555 mg 1,865 mg Nonphytate form 230 mg 400 mg 480 mg Only supplemental Mg (< 167 mg as (< 350 mg as contributes to UL supplement)
From page 134...
... is a method described by FAD/WHO (1989) for protein evaluation that is based on the essential amino acid requirements of the 2- to 5-year-old child.
From page 135...
... ~ Assumes that folate provided will be as a food fortificant and thus will be synthetic folate, which is 1.6 times more available than naturally occurring food folate. Comments Encapsulated as | NaFeEDTA suggested | Selenomethionine form Sulfate or acetate; molar ratio of Zn:phytate < 15 Does not include carotene Cholecalciferol form 0.6 mg/g PUFA | Encapsulation required | Maximum only refers to added nicotinic acid Maximum only refers to added folate Choline could be provided as lecithin
From page 136...
... Primary Packaging Each 2,100-kcal daily EFP unit will be prepared as nine equal-sized bars, each centrally scored to allow breaking into two segments. The nine bars will be individually wrapped to facilitate handling of individual bars, while reducing contamination to additional bars, through human, insect, animal, or microbial intervention.
From page 137...
... A multiple set of bars, sufficient for a 5-day supply of nine bars per day (i.e., five pouches containing nine bars each) will be packaged together and constitute the distribution unit called a "bundle." The five trilaminate pouches will be bundled into a low-density polyethylene bag to provide either a 5-day individual EFP supply or a daily ration for a family of five members.
From page 138...
... or bundles (five pouches each) may be packaged for low-altitude airdrop using appropriate package protection to simultaneously provide impact protection for the EFP and reduce the terminal velocity to a level that prevents injury to recipients on the ground.
From page 139...
... . The product must be prepared using Good Manufacturing Practices and maintain suitability as a food for the shelf life of the product.


This material may be derived from roughly machine-read images, and so is provided only to facilitate research.
More information on Chapter Skim is available.