PRODUCTION IMPLEMENTATION

With over three years invested in the devdopment and qualification of the supercritical cleaning process, the next phase of the implementation plan was cleaning of production hardware. The two key operations which had been identified early on as potoitial applications were the cleaning of end housings and the removal of bulk amounts of damping fluids from fill system fixturing. 

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The Fourier sum, involving the three dimensional FFT, does not currently run efficiently on more than perhaps eight processors in a network-of-workstations environment. On a more tightly coupled machine such as the Cray T3D/T3E, we obtain reasonable efficiency on 16 processors, as shown in Fig. 5. Our initial production implementation was targeted for a small workstation cluster, so we only parallelized the real-space part, relegating the Fourier component to serial evaluation on the master processor. By Amdahl s principle, the 16% of the work attributable to the serially computed Fourier sum limits our potential speedup on 8 processors to 6.25, a number we are able to approach quite closely. 

Design changes shall have written customer approval or waiver prior to production implementation. This requirement, although removed, is implicit in the product approval requirements. 

The Business for Social Responsibility (2002) Restricted Substances in Apparel Products Implementation Resources. [Online - accessed 1 May 2007] Available from URL http //www.bsr.org/ CSRResources/Environment/RSLImplementationResources.pdf... 

A key benefit of accurate CMP models that needs emphasis is the capability to optimize layout design before polishing. Post-CMP ILD thickness variation is a serious concern from both functionality and reliability concerns. An effective method of minimizing this effect is the use of dummy fill patterns that lead to a more equitable pattern density distribution across the chip. Evaluation of such schemes before actual product implementation has become a major use of CMP modeling [53]. Dummy fill is also being investigated for front-end processes where shallow trench isolation CMP suffers from substantial pattern dependencies. 

Draft guidance for Industry labeling for human prescription drug and biological products-implementing the new content and format requirements http // www.fda.gov/cder/guidance/6005 dft.pdf (accessed January 27, 2006). 

Elsa Reichmanis I don t believe so. Historically, the timescale has always been 10 to 15 years from research concept to product implementation. I don t think the 10-year SEMATECH road map is defining this cycle. 

Draft guidance for industry Labeling for Human Prescription Drug and Biological Products - Implementing the New Content and... 

Concurrent Technologies Corporation (CTC), through the Navy ManTech National Metalworking Center (NMC), has advanced the development of FSW in thick-section 5083, 2195, and 2519 A1 for ground and amphibious combat vehicles. Several large-scale prototypes have been completed. The work by CTC and NMC has provided a valuable transition of the technology from subscale laboratory work to full-scale prototype construction— the last major step before production implementation. 

CFR Title 21, 314—Applications for FDA approval to market a new drug (FDA, 2003b) Labeling for human prescription drug and biological products— implementing the new content and format requirements (FDA, 2006b)... 

FDA. Labeling for human prescription drug and biological products—implementing the new content and format requirements (draft) 2006b. 

Product implementation complies with aircraft and system requirements R R R A N Verification Procedures 5.5.1 ... 

Product implementation complies with aircraft and system requirements. 

The EC has harmonized fire tests for construction products, implementing Article 20 of Directive 89/106/EEC on construction products and mandating CEN to develop standards. The current classification is shown in Table 23.8. 

The organization shall maintain a record of the date on which each change is implemented in production. Implementation shall include updated documents. 

Studies and optimization of chemical formulations for polymerization reactions in MF reactors require on-chip characterization of reagents and products. Implementation of in situ characterization enables (i) exploration of the reaction variable space for high-throughput screening, (ii) opportunity for feedback control of the reaction variables, (iii) quality control of reaction products, (iv) detection of transient species, which may not exist upon their removal from the MF reactor, and (v) kinetic studies with good time resolution. 

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