Results sheet

In papemiaking, chemicals can be added either to the pulp slurry prior to sheet formation, ie, internal or wet-end addition, or to the resulting sheet after complete or partial drying, ie, surface or dry-end addition. The method chosen depends on retention and the desired effect. For example, strength additives usually are added internally if uniform strength throughout the sheet is wanted, but they are applied to the surface if the need is for increased surface strength. If an additive caimot be retained efftciendy from a dilute pulp slurry, then it is better to apply it to the surface of the sheet. 

Usually a three-bowl calender is employed wherein the rubber sheet is formed between the upper and middle bowls while the resulting sheet is simultaneously being frictioned into the substrate... 

A suggested spreadsheet for the above calculations is shown in Table 4.3. The values for residues and ash are entered from results sheets printed with columns for crucible weights, etc., unless the laboratory is equipped with computerized balances, when a more sophisticated spreadsheet could be devised. 

H20-insol soap 2.8, and product of reaction betw oleic atid and aniline 1.2%. It is blended under water and the resulting slurry is centrifuged, passed thru endless screw press and then thru heated rolls. The resulting sheets are cut into strips, or passed thru press to form cords. The insol soap consists of Mg oleate 70, Caoleate 20 Ca stearate 10%... 

Rosslyn Powders. Several smokeless powders patented in Engl in 1894-1895. One was prepd by treating nitrated tissue paper with K or Ba nitrate, starch and vaseline, previously dissolved in some volatile material such as benz. The resulting sheet was cut into strips of desired size and dried... 

Fig. 24 Schematic diagram of the formation of tubes from two different DX tiles (yellow and blue in (a)), assembling through sticky ends, represented as complementary shapes. The resulting sheets (b), labeled with biotin (black dots), can fold in register, yielding achiral tubes (c), or with shifted bonds, giving rise to helical tubes (d). The TEM images in (e, f), with scale bar 200 nm, show zigzag arrangement of biotin (bright dots), indicative of chiral structures. Adapted from [108]...

All levels of development testing for the computer system must be fully documented and provide test records in the form of approved test procedures, signed-off test result sheets, and reports. For system parameters, data, and functions that are critical to product quality and GMP compliance it is beneficial that the test procedures align with qualification test requirements, and record... 

Each test procedure and resulting test result sheet(s) should be linked by a unique test reference number and be in a logical order, particularly if a series of tests are required for similar items. This ordering method should be clearly explained. 

Each test run should be recorded on a separate test result sheet and signed and dated as a minimum by the tester and a test reviewer. All test information should be recorded on the test result sheet, or as necessary on clearly identified... 

A development test result sheet should include the following information at a minimum ... 

Calibration of the instrumentation will be performed over the complete instrument loop. During each loop calibration, all data must be documented on appropriate instrument and loop calibration sheets and submitted to the pharmaceutical manufacturer for review, approval, and record. Calibration test equipment must be traceable back to agreed-upon national standards and documented on each calibration result sheet. 

The loop test results should be recorded (a sample instrument loop check sheet has been provided for reference purposes in Appendix 23D) and included with the site test records. Checks for mechanical/electrical completeness are recorded using the upper section of the sheet and the dytramic loop test results are recorded on the lower section. The test results sheets will provide the documentary evidence essential for Installation Qualification (IQ). Representatives from the installation contractor and/or the customer will witness the final loop tests and countersign the test sheets. Any tests not witnessed must be accompanied by written confirmation from the customer that witnessing has been waived. 

The IQ is the responsibility of the pharmaceutical organization. The IQ shall define methodical inspections that verify the hardware and software installation against the design. Each inspection is conducted in accordance with a detailed inspection method and the outcome verified against unambiguous acceptance criteria. The results of the inspection must be recorded on a test result sheet, referenced to or contained within the IQ protocol. An inspection will be deemed to have passed if aU the acceptance criteria set forward have been satisfied. Table 31.15 provides the typical contents of an IQ. 

Figure 297(a) depicts the production of a checkerboard sheet. D-shaped briquette pockets are positioned alternately in a checkerboard fashion. The resulting sheet is passed between a smooth pair of rollers, the gap of which is set to a width corresponding to pocket depth plus gap width. While the sheet is squeezed, the shear forces created in the land areas will separate the briquettes from one another. 

The data reported by the laboratories should be comparable and will be treated by the organiser of the study. Therefore, unambiguous information must be available to the organiser to prepare the report of the exercise. This may include tables for raw data, data corrected for dry mass, recovery for organic and organo-metallic determinations, linear response of the detector, calibration range, data expressed on a fat content basis etc. Such results sheets are also illustrated in Annex 12.1. 

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