Intent, defined

Intention—defines how the part or process is expected to operate. 

Intention the intention defines how the particular part of the process was intended to operate the intention of the designer. 

In such strategies, two comonomers are intentionally defined as 0 and 1 bits. The monomer T is a thymine nucleotide, which is used to start the sequence and facilitates the pol rmer characterization, (b) Extended-ASCII encoded text that was implemented in the primary structure of a polymer using the monomer-based digital code, (c) Schematic representation of the primary structure of the corresponding sequence-coded polymer and its characterization by negative mode electrospray mass spectrometry (ESI-MS). 

The acronym LASER (Light Amplification via tire Stimulated Emission of Radiation) defines the process of amplification. For all intents and purjDoses tliis metliod was elegantly outlined by Einstein in 1917 [H] wherein he derived a treatment of the dynamic equilibrium of a material in a electromagnetic field absorbing and emitting photons. Key here is tire insight tliat, in addition to absorjDtion and spontaneous emission processes, in an excited system one can stimulate tire emission of a photon by interaction witli tire electromagnetic field. It is tliis stimulated emission process which lays tire conceptual foundation of tire laser. 

In some cases, whole parts of the protein are missing from the experimentally determined structure. At times, these omissions reflect flexible parts of the molecule that do not have a well-defined structure (such as loops). At other times, they reflect parts of the molecule (e.g., terminal sequences) that were intentionally removed to facilitate the crystallization process. In both cases, structural models may be used to fill in the gaps. 

The influence of a particular dielectric on the capacitance of a condenser is conveniently assessed by the dielectric constant, also known as the relative permittivity or rarely specific inductive capacity. This is defined as the ratio of the relative condenser capacity, using the given material as a dielectric, to the capacity of the same condenser, without dielectric, in a vacuum (or for all practical intents and purposes, air). 

ISO 8402 1994 defines quality policy as the overall quality intentions and direction of an organization with regard to quality, as formally expressed by top management it adds that the quality policy forms one element of corporate policy and is authorized by top management. The quality policy that is required to be defined is therefore the corporate quality policy and not lower-level policies. However, there are different types of policy and it is important that they are not confused so that a policy purporting to be a... 

Declare the intention to utilize defined processes throughout the organization in order to achieve more predictable results. 

Quality plans are needed when the work you intend to carry out requires detailed planning beyond that already planned for by the quality system. The system will not specify everything you need to do for every job. It will usually specify only general provisions which apply in the majority of situations. You will need to define the specific documentation to be produced, tests, inspections, and reviews to be performed, and resources to be employed. The contract may specify particular standards or requirements that you must meet and these may require additional provisions to those in the quality system. Although ISO/TS 16949 requires the plan to include customers requirements, the intention is not that these requirements are reproduced if provided in a documented form by the customer, but that a cross reference is made in the plan together with any other relevant specifications referred to in the contract. However, when constructing the plan, it would make sense to refer to specific customer requirements and provide a response that indicates your intentions regarding those requirements. 

The quality plan would be a logical place for such controls to be defined but clause 4.2.3 does not specifically refer to subcontractor controls. Any intention that they be defined in the quality plan is hidden in 4.2.3.1(b) where it requires you to give timely consideration to the identification and acquisition of any controls etc. Some companies produce a Quality Assurance Requirement Specification to supplement ISO 9001 and also produce a Subcontractor Surveillance Plan. In most other cases the controls may be defined on the reverse side of the purchase order as standard conditions coded and selected for individual purchases. 

These examples are intentionally very broad-based to help expand your thinking about your company s management systems. While they address some very different issues, they all share the 22 characteristics of a management system as defined by CCPS, whether implicitly or explicitly. 

Regarding corrective actions, the regulation states The employer shall establish a system to promptly address and resolve the incident-report findings and recommendations. Resolution and corrective actions shall be documented. The regulation does not define promptly in definitive terms, but the intent is that all corrective actions must be implemented immediately. 

The procedures for obtaining a Community marketing authorisation are defined in EC Regulation No. 726/2004. The types of human-use medicinal products for which the procedure may be used are shown in Eigure 6.14. The applicant should notify the EMEA of their intention to submit an application at least 7 months... 

From a quantitative perspective, each peak is defined by two parameters, i.e. the position of its baseline and the retention time boundaries, with those derived by the computer system being shown in Figure 3.27. It is not the intention of this present author to discuss how these have been determined but simply to point out that their positions may have a significant effect on the accuracy and precision of any quantitative measurements, especially, as in Figure 3.27, when the baseline is not horizontal and the signals from each of the components are not fully resolved. It is usual for the software to allow the analyst to override the parameters chosen by the computer to provide what they consider to be more appropriate peak limits and/or baseline positions. 

The intention of this chapter is to provide a general survey on the preparative methodologies for the size- and shape-selective synthesis of metallic nanoparticles that have emerged from the benches of chemical basic research during the last few decades and become established as practical standard protocols. Industrial scale-up, however, has only just started to test the economic viability of these procedures and to determine whether they can meet the challenges of a number of very specific applications. The commercial manufacture of such thermodynamically extremely unstable nanoparticles in defined sizes and shapes on the kilo-scale is still confronted by a number of major problems and it remains to be seen how these can be solved. 

The next few steps are very similar to those required in any software project. One of the first stages is the clear definition of the knowledge domain. It must be clear which problems the expert system must solve. It is at this stage not the intention to define how this can be done. Clarity and specificity must be the major guides here. Fuzziness at this stage will, more than in classical software projects, have to be paid for later when different interpretations cause misunderstandings. Equally important is the clear definition of the end user(s). An expert system set up as decision support tool for professionals is totally different from an expert system that can be used as a training support for less professional people. 

The activation energy Ea - defined as Ec - Ey for the conduction band (and analogously for the valence band), can be used to assess the presence of impurities. Due to their presence, either intentional (B or P dopant atoms) or unintentional (O or N), the Fermi level shifts several tenths of an electron volt towards the conduction or the valence band. The activation energy is determined from plots of logafT) versus 1/7, with 50 < 7 < 160°C. For undoped material Ea is about 0.8 eV. The Fermi level is at midgap position, as typically Eg is around 1.6 eV. 

The e-records rule uses many terms that must be understood to grasp fully the intent of the rule. FDA defines electronic records as any combination of text, graphics, data, audio, pictorial, or other information presented in digital form that is created, modified, maintained, archived, retrieved, or distributed by a computer system . A printout of a computer file is not the actual electronic record itself Electronic records include other relevant data, such as which user made a change, the time and date that the change was made, etc. 

O Intravenous factor replacement with recombinant or plasma-derived products to treat or prevent bleeding is the primary treatment hemophilia. Primary prophylaxis is defined as the regular administration of factor concentrates with the intention of preventing joint bleeds.4 The rationale for primary prophylaxis is that individuals with factor levels of greater than 0.02 unit/mL (2 IU/dL) rarely suffer from spontaneous bleeds and arthropathy. Therefore, to maintain a trough level above this might convert severe hemophilia to moderate disease, with the abolition of joint bleeds and the associated arthropathy.5... 

Health care providers use a multimodality approach including surgery and chemotherapy in the initial treatment of ovarian cancer with a curative intent. Although most patients will achieve a complete response initially, more than 50% of cancers will recur within the first 2 years,2,35 Complete response to treatment is defined as no evidence of disease can be detected by physical examination or diagnostic tests, and patient has a normalized CA-125 value. 

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