Technical files defined

Pattern 16.7, Implement Technical Architecture Define major technical components of your design as an architectural collaboration. These components might be GUI, business logic, persistence (database or file system), communications, and other middleware elements. 

About the materials, PED defines the pressure-retaining parts for the valves in the technical file of each valve type. Typically, for an SRV, this would be body, bonnet, disc and nozzle but could be different depending on the type of SRV. These parts must satisfy material requirements and have an EN10204 3.IB (now 3.1) material certificate, and are therefore traceable. 

An invention possesses novelty when the technical knowledge for which the patent protection is sought is not included in the state of the art. Not in the state of the art is usually defined as all the information not available to the public, in any form of disclosure - oral, written, digitized, use/ exploitation, among others - at the time of filing the patent application. Absolute novelty is adopted by most countries, meaning that which has not been disclosed anywhere in the world. 

This can be accomplished by allowing the user to define which metadata he wants to be represented in the file tree view. From a technical point of view, metadata are constructed with a meta-key that represents the name or category of the data and a value. By changing the metakey structure in his current session, each user would be able to see (1) only the documents he is interested in and (2) the files categorized in an appropriate sequence. Figure 8.4 shows an example of different metadata structures displayed for different users. 

Novelty and Nonobviousness To be patentable, an invention must be new, useful and not obvious. Section 102 of the Act defines novelty quite technically. An invention is not novel if, before the applicant s invention, the invention was (a) known or used by others in this country ( 102(a)) (b) patented or described in a printed publication anywhere in the world before the applicant s invention ( 102(b)) (c) described in a patent on a United States patent application filed before the applicant s own invention ( 102(e)) or (d) made in this country by another who has not abandoned, suppressed or concealed it ( ... 

The Multi-Agency Radiation Survey and Site Investigation Manual (MARSSIM) describes the quality system as consisting of all efforts devoted to produce quality results that are authentic, appropriately documented, and technically defensible (EPA, 2000c, Chapter 9). The purpose of the quality manual or QAP is to describe, in a single document, all elements of the quality system. This includes all laboratory policies regarding quality and all of the QA measures implemented by the laboratory. Some records may be included in the QAP itself, while others are filed as specified in the QAP. The QAP defines every element of laboratory operation and represents the laboratory s commitment to quality. The interconnected elements of QA policy that must be included in the QAP are... 

Quality control is defined as an overall system of technical activities that measures the attributes and performance of a process, item, or service against defined standards to verify that they meet the stated requirements established by the client or customer. QA is a management function, whereas QC can be viewed as a laboratory function. A laboratory must have a written QA document on file, whereas a record of certified reference standards that are properly maintained implies that QC is in place. Much of what has been discussed in this chapter falls under the definition of QA. 

All test chemicals should be filed in a central repository after receipt and proper accessioning. A chemical safety data sheet (Figure 2) should accompany all compounds with proper storage conditions defined. The chemical repository should be an area of maximum safety precautions and limited access. Generally, one person with full chemical safety gear should dispense premeasured samples of all chemicals to the technical staff. These samples should be coded to ensure unbiased evaluation. Safety information should accompany the sample into the laboratory. 

---