Control strategy summary

Industrial Data Sheets (Summaries of toxic data and control strategies on many industrial chemicals)... 

National Drug Control Strategy FY 2003 Budget Summary. Washington, D.C. The White House, 2002. 

Office of National Drug Control Policy, 2006. National Drug Control Strategy FY 2007 Budget Summary February 2006. http //www.whitehousedrugpolicy. gov/publications/policy/07budget/. 

Office of National Drug Control Policy, 2005. The President s national drug control strategy, FY 2006 budget summary, February 2005.http //www. whitehousedrugpolicy.gOv/publications/policy/06budget/dhhs.pdf. 

Kumar, N., Gammell, P., and Clynes, M. (2007) Proliferation control strategies to improve productivity and survival during CHO based production culture a summary of recent methods employed and the effects of proliferation control in product secreting CHO cell lines. Cytotechnology, 53, 33-46. 

In the preceding sections quantum dynamical methods to describe the propagation of electronic and vibrational wavepackets have been outlined as well as a summary of the OCT. In the next sections we demonstrate the potential of OCT to guide vibrational wavepackets on coupled electronic potential energy surfaces. We will extend the control strategies to include the steering of electronic wavepackets explicitly. 

In summary, the ATP example shown here describes critical method performance requirements, that is, those characteristics that have a direct impact on the ability of a method to quantitate an analyte. LC-method attributes such as peak resolution, linearity, and efficiency, are not included. Although they are important features of an LC method and should be evaluated and incorporated into the control strategy as required, they do not provide a direct measiu-ement of the ability of a method to accurately quantitate an analyte and should not appear in the ATP. 

Regarding stereoselective control elements, some of the most important and updated methods and strategies, have been already discussed in Chapters 8 and 9 (see also the Summary given below). 

It is our intention to present strategies based on chemically induced phase separation (CIPS), which allow one to prepare porous thermosets with controlled size and distribution in the low pm-range. According to lUPAC nomenclature, porous materials with pore sizes greater than 50 nm should be termed macroporous [1]. Based on this terminology, porous materials with pore diameters lower than 2 nm are called microporous. The nomination mesoporous is reserved for materials with intermediate pore sizes. In this introductory section, we will classify and explain the different approaches to prepare porous polymers and to check their feasibility to achieve macroporous thermosets. A summary of the technologically most important techniques to prepare polymeric foams can be found in [2,3]. 

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