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A good operation instruction must contain at least the following points: (i) equipment description, containing the function of the equipment, name, code, serial number, model, manufacturer, accessories, dimensions, power source, connections, and component descriptions; (ii) function, containing a description of a procedure of how to handle the equipment, and all the steps required and options; (iii) calibration procedure, described in detail and providing the calibration periodicity; (iv) maintenance, a simple and easily maintenance procedures should be available; (v) cleaning described in detail; and (vi) security procedures Equipment System Validation The GMP has special features regarding the equipment, setting several points for the validation, such as design quali cation, installation quali cation, operational quali cation, and performance quali cation Each point must be given in a different document, so four documents must be generated for each equipment Without any of these documents, the equipment cannot be considered adequate for GMP purposes.

25.3 CONCEPTUAL METHODS OF INTEGRATING CAD WITH DICOM PACS AND MIII Integration of CAD with DICOM PACS or MIII can have four approaches. In the rst three described below, the CAD is connected directly to the PACS. The fourth approach is a separate CAD server that can be connected to either the PACS or the MIII, or both. 25.3.1 PACS WS Q/R, CAD WS Detect

Figure 15.1. Potential energy surfaces for bound states, S0 and S1 , and a dissociative state, S2 .

Nearly any wireless device can be improved by adding a better antenna. So if you want to improve your signal transmission or reception, it is worth considering an antenna upgrade. Now that you know what different antennas exist, let s consider when you would want to select one type of antenna over another. Table 12-1 has some recommendations.

Type the message that you want to send in the lower pane. When you re done, click Send. The message is sent to your buddy. The message that you typed also displays in the upper pane. When your buddy responds, his message also appears in the upper pane. In this way, you see the conversation happen in sequence. (Obviously, your buddy needs to be logged in. You can see his status in the Buddy List window.) If a buddy initiates a conversation with you, a window appears asking you if you want to accept the message. If you do, the chat window opens with your buddy s message in it. When you are done chatting, click on the Conversation menu and select Close. The chat window disappears.

GMPs do not refer equipment validations; nonetheless, they refer these four items, and therefore, equipment can only be considered validated after the approval of these four documents Equipment validation is not reliable, and several special features are required instead GMP is concerned with several procedures before the equipment is placed into the service After entrance into service, maintenance and calibration must be made periodically The following focuses on the procedures required for new equipment to enter into service Design Quali cation When a pharmaceutical industry intends to purchase new equipment, it must rst know and de ne what type of equipment and which speci cations it must have Speci cations must be set taking into account speci c requirements of the company or facility All the speci cations of the equipment must be reviewed This is called design quali cation.

If the closest point of approach (CPA) becomes less than the user de ned value, the target blinks, an audio warning sounds and the display includes the value of the CPA and the elapsed time until the CPA. A list of all the targets can be displayed on the screen, all the data for each target can be viewed or alternatively if a target is clicked, then its data can be displayed.