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A carbon nanotube is a single molecule of graphite, a large macromolecule, shaped in a cylindrical sheet (a hexagonal lattice of carbon); the ends of the cylinder are terminated by hemispherical caps See Figure 43; Figures 16, 35, 36, 37, and 312 also provided additional pictorial views The molecular formulation of single-wall carbon nanotubes requires that every atom be in the right place; this structure provides single-wall carbon nanotubes with their unique properties Carbon-based SWNT can be metallic or semiconducting; they o er interesting possibilities to create future nanoelectronics devices, circuits, and computers Carbon nanotubes are a macromolecule of carbon (one can visualize this as a sheet of graphite rolled into a cylinder; graphite looks like a sheet of chicken wire, a tessellation of hexagonal rings of carbon) Di erent kinds of nanotube are de ned by the diameter, length, and chirality (twist).

Employee name Employee identi cation Personal quali cation pathway, including training programs that need to be completed and targeted completion dates Results of training programs completed

In addition to single cylindrical SWNTs nanotubes, one also has multiple-wall nanotubes (MWNTs) with cylinders inside the other cylinders The length of the nanotube can be millions of times greater than its.

Changes are being made in the manufacturing process and chemistry of a drug product following approval and continue throughout its life Depending upon foreseen (or unforeseen) requirements, there can be changes in the raw materials, process, equipment or manufacturing site, and batch size which ultimately affect quality attributes of a drug or nished product Therefore, there is a need to anticipate and fully evaluate the impact of any kind of change on the quality of a drug or nished product There can be several reasons for these changes, such as changed market requirement affecting batch size, new source of raw material, change in manufacturing process, upgrades of packaging material, or shifting to a new analytical methodology The intensity of the adverse effect produced by a particular change depends on the type of dosage form.

[6] S. Haykin, M. Sellathurai, Y. de Jong, and T. Willink, Turbo-MIMO for Wireless Communications, IEEE Communication Magazine, pp 48 - 53, October 2004.

Despite the challenges and problems with VoIP and SoIP, the adoption has a strong drive, primarily because of unification of different networks and the promise of a single all-purpose communication application. Both of these promises are what corporations like, because they can potentially lead to reduced IT costs and increased user productivity. Together they also support the do more with less tenet.

For example, a change in the inactive ingredient beyond a certain range will have more effect on a modi ed-release (MR) dosage form than it would on an immediate-release (IR) dosage form, where bioavailability is not rate limiting Likewise, a change in the primary packaging of liquid parenteral may have more pronounced effect on its effectiveness than it would have on a solid dosage form Hence, depending upon the intensity of change or the adverse effect it may have on the critical parameters of a dosage form, reporting requirements to regulatory authorities also vary A drug or drug product may experience many changes during its life cycle These changes may have an adverse effect on the overall safety and effectiveness of the drug or drug product.

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