Narrow Your Results
1.1 This test method covers determination of the amount of residual solvents released from within a packaging material contained in a sealed vial under a given set of time and temperature conditions and is a recommended alternative for Test Method F151. 1.2 This test method covers a...
4.1 Single-use systems (SUSs) used for biopharmaceutical manufacturing must maintain sterility and product quality of the fluid inside. Such articles or systems should therefore be validated as providing an effective barrier against microbial ingress. The microbial barrier properties of a SUS may...
This test method is applicable to the determination of ethoxyl or hydroxyethoxyl substitution in cellulose ether products by a Zeisel gas chromatographic technique. The equipment and materials to be used shall include reagents, gas chromatograph, electronic integrator, column, syringe, reaction...
5.1 In order to calculate the volatile organic content (VOC) of paints containing EPA exempt solvents, it is necessary to know the acetone, methyl acetate, or parachlorobenzotrifl
1.1 This test method covers the determination of glycol based antifreeze for in-service engine oil by derivative headspace/gas chromatography. 1.2 Sample is derivatized in-situ directly in a headspace sampling vial prior to vapor phase extraction and injection into a gas chromatograph. 1.3...
5.1 This test method evaluates, under carefully controlled conditions, the changes in the mass of a test specimen on exposure under vacuum to a temperature of 125 °C and the mass of those products that leave the specimen and condense on a collector at a temperature of 25 °C. 5.2 The 24 h test time...
An oil sample is placed into an open top glass vial which is then inserted into a stainless steel pressure vessel. The vessel is then sealed, pressurized, and placed into a heated aluminum block bath for 18 hours. At the end of the 18 hour time period, the vessel is removed from the heat...
5.1 The carbon residue value of the various petroleum materials serves as an approximation of the tendency of the material to form carbonaceous type deposits under degradation conditions similar to those used in the test method, and can be useful as a guide in manufacture of certain stocks....
Abstract: Packaging-performanc
This Protocol is intended to cover certification of drug testing sample collection and security equipment, including urine, whole blood, and serum blood sample collection, and encompasses required testing methods, design, and material requirements for this equipment. This Protocol covers only the...
5.1 This guide is applicable for all ignitable liquids as defined by Test Method E1618. 5.2 This guide is applicable to solid and liquid samples (burned and unburned), which are packaged in a closed vapor-tight container (typically a can, fire debris bag, jar, or vial). 5.3 This guide is to...
5.1 This guide is applicable for all ignitable liquids as defined by Test Method E1618. 5.2 This guide is applicable to solid and liquid samples (burned and unburned), which are packaged in a closed vapor-tight container (typically a can, fire debris bag, jar, or vial). 5.3 This guide is to...
This document specifies the characteristics of sterile and ready for filling empty glass vials for injectable preparations, including the minimum requirements of materials, packaging systems and analytical test methods.
This document specifies the characteristics of sterile and ready for filling empty glass vials for injectable preparations, including the minimum requirements of materials, packaging systems and analytical test methods.
This document specifies the form, dimensions and capacities of glass vials for injectable preparations. It also specifies the material from which such containers are made and the performance requirements of those containers. This document is applicable to colourless or amber glass containers...
4.1 Single-use systems (SUSs) used for biopharmaceutical manufacturing must maintain sterility and product quality of the fluid inside. Such articles or systems should therefore be validated as providing an effective barrier against microbial ingress. The microbial barrier properties of a SUS may...
This document specifies test methods for efficiency of chemically or physically treated textile products against house dust mites. For the products treated by chemicals against house dust mites, the test methods specified in a) to c) are applied. For the physically treated products, the test method...
