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Data requirements can also be identified in the contract via special contract clauses (e.g., DFARS), which define special data provisions such as rights in data, warranty, etc. SOW guidance of MIL-HDBK-245D describes the desired relationship: "Work requirements should be specified in the SOW, and all data requirements for delivery, format, and ...
The CAPE-OPEN, European Union funded, project was established in 1997. [1] The project involved participants from a number of companies from the process industries (Bayer, BASF, BP, DuPont, French Institute of Petroleum (IFP), Elf Aquitaine, and Imperial Chemical Industries (ICI)) together with 15 partners including software vendors (Aspen Technology, Hyprotech Ltd, QuantiSci and SimSci]) and ...
Mandatory country-of-origin labeling of food sold in the United States; Personal Responsibility in Food Consumption Act; Public Law 114-214, regulating GMO food labeling; Pure Food and Drug Act; Standards of identity for food; Title 21 of the Code of Federal Regulations; United States v. Correll; United States v. Ninety-Five Barrels Alleged ...
Some specimen types also require special treatment, such as immediate mixture with an additive, or storage at a certain temperature. [5] After extraction , all specimen containers must be labeled with at least two of the following identifiers (at the time of collection): patient's name, date of birth, hospital number, test request form number ...
[3] Section 4205 is an amendment to the nutrition labeling requirements of Section 403(q)(5) in the Federal Food, Drug, and Cosmetic Act (FFDCA), under the Nutrition Labeling and Education Act of 1990 (NLEA). Section 4205 mandates labeling nutrition information for foods at chain restaurants and vending machine items to help consumers make more ...
A biological specimen (also called a biospecimen) is a biological laboratory specimen held by a biorepository for research. Such a specimen would be taken by sampling so as to be representative of any other specimen taken from the source of the specimen. When biological specimens are stored, ideally they remain equivalent to freshly-collected ...
The Fair Packaging and Labeling Act is a U.S. law that applies to labels on many consumer products. It requires the label to state: The identity of the product; The name and place of business of the manufacturer, packer, or distributor; and; The net quantity of contents. The contents statement must include both metric and U.S. customary units.
The requirements under sections 4, 5, 6, and 10 of the CPLA (which deal specifically with requirements regarding labels, advertising, packaging, and net quantity information) do not apply to any prepackaged products that fall under the labelling requirements of any of the following: [9] Feeds Act; Fertilizers Act; Seeds Act; Pest Control ...