Inspection version

Industrial User Inspection and Sampling Manual for POTWs (Diskette Version and Printed Appendices), April 1994 ERIC W493 NTIS PB96-502646. 

Ultrasonics has been utilised in several versions of pipeline inspection vehicle see section below). The use of ultrasonics for detection of hydrogen damage in steels has been reported"". ... 

Intelligent vehicles have been developed with arrays of ultrasonic probes for pipeline inspection — one commercial version contains 512 ultrasonic sensors. 

One of the disadvantages of the porcelain Buchner funnel is that, being of one-piece construction, the filter plate cannot be removed for thorough cleaning and it is difficult to see whether the whole of the plate is clean on both sides. In a modern polythene version, the funnel is made in two sections which can be unscrewed, thus permitting inspection of both sides of the plate. 

Food colorants play an important role in quality perception. Color is often the first notable characteristic of a food and it influences the expectations of consumers buying the product and also influences food handlers who make quality-related decisions, for example, during visual inspections." More specifically, color predetermines our expectations and perceptions of flavor and taste. " Color is interrelated with flavor intensity (detection threshold), with sweetness and salinity sensations, and also with our susceptibilities to and preferences for products. For example, consumers perceived a strongly red-colored strawberry-flavored drink to be sweeter than a less colored version, and yellow was associated with lemon and pink with grapefruit, but by reversing the colors, flavor perception changed." If food color is not appealing, consumers will not enjoy the flavor and texture of the food. ... 

Floyd, Joel, and Conrad Krass. New Pest Response Guidelines Huanglongbing, Citrus Greening Disease, Version 1.1. United States Department of Agriculture, Animal and Plant Health Inspection Service, May 10,2006. 

Manufacturing sites within Australia must comply with the Australian Code of GMP for Medicinal Products - August 2002, which is based entirely on the international standard Guide to Good Manufacturing Practices for Medicinal Products, Version PHl/97 (Rev.3) 15 January 2002, published by the Pharmaceutical Inspection Cooperation Scheme (PIC/S). The ICH GMP Guide for Active Pharmaceutical Ingredients has also been adopted. 

The historical file of SOPs documents what SOPs were in effect at any time during a laboratory s history. Because FDA inspection of a study often occurs years after the completion of that study, the historical file of SOPs will be of special use to an FDA inspector. Including the effective date on the SOP itself will aid in maintenance of the historical file and will also make it easier to ascertain if any one SOP manual contains the current version of any individual SOP. Accessory documentation of effective dates (e.g., in the transmittal memo for the distribution of SOPs) is permissible but not recommended. 

The approaches to this problem follow along two general lines. In the first approach, one computes derivatives of the dipole moment with respect to the applied field and relates them to the terms in the polarization expansion of equation 8. Inspection of equation 8 suggests that the second derivative of the dipole moment with respect to the field gives p. The choice of the exact form of the Hamiltonian, which incorporates the optical field and the atomic basis set, determines the accuracy of this procedure. In one popular version of this approach, the finite field method, the time dependence of the Hamiltonian is ignored for purposes of simplification and the effects of dispersion on p, therefore, cannot be accounted for. 

Standard operating procedures (SOPs) are required for all routine activities that are critical to the successful outcome of the study including quality assurance procedures and inspections. Most of the SOPs for the field activities are written by the field scientists with guidance from the Quality Assurance Section. For the field activities, it is required that at each site there be SOPs for such things as how field plots are established and the plot boundaries marked, the maintenance of sample freezers, how to calibrate and maintain chemical balances and chemical application equipment, and how to obtain test chemicals. If an SOP for a critical item of equipment is not available, the study would be considered to be not in compliance with the principles of the GLP guidelines. The distribution of SOPs is carefully controlled so that when an SOP is changed, all outdated copies can be exchanged for the new version. 

The steel version comprises a two-piece housing, on request with an inspection window. Thin-wire erosion is used for microfabrication of the tiny cogs which served as inlet structures to achieve the multi-lamination (see Figure 1.87). High-speed... 

All of this is fairly simple if your product is a generic version nevertheless, the information must be contained in a concise report and be available to the FDA during inspection. 

Guia de Inspecciones de Sistemas deAgua de Alta Purez English version Guide to Inspections of High Purity Water Systems. (Issued July 1993)... 

The sample preparation kit (Picture 2) holds all equipment necessary to prepare the samples for GC/MS analysis on-site in four transport boxes (flight cases). It contains everything from the pH paper to the laboratory coat including the chemicals to conduct the sample preparation procedures. A reduced version of the sample preparation kit packaged in two pelli cases is available for inspections where this will suffice. 

Therefore, the information obtained, through onsite GC/MS analysis about the identity of compounds present in a sample should be restricted to chemicals relevant to the aim of the inspection. This is achieved by operating the instrument in a specially developed blinded mode, which shows neither the chromatogram nor mass spectra during or after the chromatographic run. Additionally, if the analysis is conducted in blinded mode, the only available postprocessing software is a specifically developed on-site version of AMDIS (Automated Mass Spectral Deconvolution and Identification System). This software works only with the OCAD, which contains only compounds relevant to the CWC thus, it reports exclusively the presence of compounds for which spectra are in this database library. 

The on-site version of AMDIS is a 16-bit Windows application running under OS2 operating system of the Dolch PC. This version of AMDIS was specially designed by NIST (National Institutes of Standards and Technology) for OPCW on-site analysis use. Its role in the postprocessing of analysis data is equivalent to the role of the blinded mode software in regard to the general control of the instrument and the acquisition of the data restrict the information on the identity of chemicals present in the sample to chemicals that are only relevant to the inspection aim. 

The electronic MS on-site databases are prepared from the certified electronic version of the OCAD (e-OCAD). This version is compiled using the NIST programs (NIST MS Search/Analysis and AMDIS) and is in the form of a NIST MS Database. The e-OCAD does not contain Gas Chromatography retention indices (GC(RI)) that are required for on-site use. To create an electronic MS onsite database, the certified version of e-OCAD, which at the moment contains only MS data, is merged with the certified (GC(RI)), which is in an excel spreadsheet. After merging these data, an AMDIS version of the database is created, which is compatible with the AMDIS software used by the on-site GC/MS equipment (for more details on the software, refer to Chapter 2 and Chapter 4) (5). The MS on-site database can be sent for an inspection as a whole database or as an extract of the whole database. AMDIS is software that is used by the GC/MS on-site equipment... 

---