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After you ve set your upload preferences, you can upload your site to the WebDAV server. Initially, only one person on a team uploads the site. Once it s uploaded, the rest of the team open their local copies, connect to the copy on the WebDAV Server, and synchronize their local (hard drive) copies to the one on the server in order to join the collaboration. You don t have to have general WebDAV preferences entered in order to upload your site or use WebDAV in any way. You only need site-specific WebDAV preferences to proceed. Follow these steps to upload the site: 1. With the Site Window active, click the WebDAV server Connect/Disconnect button in the toolbar (or choose Site WebDAV Server Connect/Disconnect). The button will not be active if don t have a Site Window open and active. Click the Site Window to bring it forward.

. Controlling the packet domain network access connections, such as attaching to and detaching from the packet domain network. . Controlling the attributes of an established network access connection, such as activation of a PDP address. . Controlling the routing path of an established network connection in order to support user mobility. . Controlling the assignment of network resources to meet changing user demands.

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To make a maximum use of the available numerical libraries and apply them dynamically on each application execution phase, we need to pro le the application characteristics at runtime. At runtime, different application phases can be abstracted as a skeleton in which information, such as optimal algorithm on which platform, what is this phase about, it is an I/O phase or a linear system solving phase, and so on is stored. Though there are unlimited scienti c applications in the community, the total number of the skeletons is limited. We need to build a knowledge base to identify classes of applications and store all the skeletons and develop an optimal numerical algorithm for each skeleton. At runtime, we can retrieve information from this knowledge base to instruct the application to switch algorithms based on their current physical phases. Therefore, to optimize any scienti c application using our techniques, the following major steps will be enforced: 1. Identifying Phases: At runtime, we monitor the application execution and identify different phases based on the physical properties of the application. 2. Planning Phase: The monitored physical phases are fed into planning engine in which corresponding optimization techniques will be decided. Planning

When you copy or drag text from another source, such as a word processor, character and paragraph formatting will be lost. When you copy or drag text from within GoLive, character formatting remains intact.

Understanding external references Attaching external references Editing external references from within your drawing Controlling the display of external references Managing external references

This section outlines the basics of SQL syntax. Real-life examples are used to explain select statements and make them easier to understand. This section is meant to serve as both a quick reference and an introduction to terms that you will be learning later.

For a complete and current list, go to www.iana.org/assignments/ port-numbers. Port Number 0 1 5 7 20 21 22 23 25 53 67 68 69 80 101 107 109 110 115 118 123 135 143 161 162 166 179 213 220 Description Reserved TCP port service multiplexer Remote job entry Echo FTP data FTP control SSH Telnet SMTP DNS BOOTP/DHCP server BOOTP/DHCP - client TFTP HTTP NIC host name server Remote Telnet service POP2 POP3 SFTP SQL NTP DCE endpoint IMAP SNMP SNMP trap Sirius BGP IPX IMAPv3 Applicable Protocol TCP and UDP TCP and UDP TCP and UDP TCP and UDP TCP TCP TCP and UDP TCP and UDP TCP and UDP TCP and UDP TCP and UDP TCP and UDP TCP and UDP TCP and UDP TCP and UDP TCP and UDP TCP and UDP TCP and UDP TCP and UDP TCP and UDP TCP and UDP TCP and UDP TCP and UDP TCP and UDP TCP and UDP TCP and UDP TCP and UDP TCP and UDP TCP and UDP (continued)

legal basis for GMP in the EU [14] The actual GMP code with detailed written procedures is published in The Rules Governing Medicinal Products in the European Union, volume 4 The current set of the EU GMP code was rst introduced in 1989 consisting of nine chapters covering the general requirements of GMP and one annex on the manufacture of sterile drug products Since then the EU GMP code has been revised many times and several new annexes have been issued [15] In addition to the GMP code, the EU has also published several other guidelines concerning the quality issues of drug production in The Rules Governing Medicinal Products in the European Union, volume 3A [16] As shown in Tables 3 5, the EU GMP code is presented in two parts of basic requirements and 18 annexes.

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