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A BrainLab workstation for SRT/SRS has its own storage for the plans performed at its workstation For conventional radiotherapy the treatment plans are stored in the conventional treatment planning system (TPS) and the treatment records in another information system A patient whose treatment involves all three workstations will have treatment information in three different places Currently such treatment information is normally linked by a paper record or folder of the patient This has not taken into account the hardcopy lms of images that are stored separately in the lm library, as is very common in radiotherapy departments Were the paper record lost, then the patient treatment information would be disintegrated Using the DICOM and DICOM RT standards, the multimedia ePR system integrates patient information from different systems and.

inline-applied class adds to your page as opposed to regular HTML, which would fully list every single attribute applied to the text. A type of pseudo-class exists that uses a descriptive word at the start of the class, so the class becomes something like body.main or body.sbar. However, GoLive doesn t support this as a selector. In GoLive, always make sure you begin your class selector with the dot/period (.).

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The production of drug products (medicines) in New Zealand is controlled under the Medicines Act 1981, which states that a drug manufacturer is not allowed to manufacture drug products without a manufacturing license issued by the licensing authority. In order to obtain a manufacturing license the applicant must satisfy the licensing authority with respect to the proposed manufacturing premises and equipment, which must be suitable and adequate for the manufacture of drugs. Moreover, the applicant must show that adequate arrangements have been made or are to be made for the making, maintaining, and safekeeping of adequate records with reference to the drug products that are to be manufactured [29]. The authorities (Medsafe) require that any drug manufacturer who plans to manufacture drug products for sale in New Zealand must deliver evidence of GMP compliance for the manufacturing site. Copies of appropriate certi cates, manufacturing licenses, or reports issued by a regulatory authority whose competence is recognized by Medsafe are accepted as proof of GMP compliance [30]. As shown in Table 10 New Zealand s own GMP code consists of ve parts. The rst part covers the manufacture of drug products and the second part the manufacture of blood products. Part 3 covers compounding and dispensing, including compounding of sterile drug products. Part 4 deals with wholesaling and Part 5 with product recalls. Parts 4 and 5 are combined in one document [31]. 2.1.2.8 South Africa

which causes a reduction in the intensity of the re ected light which can be detected. Inspection of Equation (3.52) shows that K sp is highly dependent on the refractive index of the medium above the metal lm. This holds up to a distance of approximately 300 nm above the metal. Any process altering n s can be sensitively detected by SPR so the technique has found applications in the study of kinetics and thermodynamics of binding processes (e.g. protein-ligand, protein-protein). Because SPR only reports on events <300 nm above the metal layer, it gives meaningful measurements of binding processes in real time, over a wide dynamic range with direct detection and no requirement for labels or special optical characteristics in the samples studied.

8.7. CONCLUSIONS As mentioned in the introduction of this chapter, the examples examined demonstrate the versatility and usefulness of the Schlieren techniques and the related phase modulation tests. Of course, the choice of any particular test depends on the circumstances.

One advantage of deleting the objects is that their disappearance confirms that you selected the right objects. If you make a mistake, or if you want to change the block in some way, you can redefine it. If you just created the block, use UNDO and make any necessary changes. If you created the block earlier, follow these steps: 1. Insert the block and explode it. (Exploding is covered later in this chapter.) 2. Make the desired changes and repeat the process of defining the block, using the same name for the block.

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