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Figure 6.3 Two digital mammograms before and after the background removal providing immediate image compression. (A) A large breast occupies most of the image. (B ) Background removed image, compression ratio 3.1:1. (C ) A small breast occupies a small portion of the image. (D) Background removed image, compression ratio 6.3:1; (Courtesy of Jun Wang)

Although most printer manufacturers now offer Windows drivers, those drivers aren t always perfected. Sometimes you must get seriously down and dirty by using an older printer DLL (dynamic link library, a basic component of Windows) with a later printer driver. If you encounter a Windows-related printing problem, your first cry for help should be to your printer manufacturer s Web site or tech support line. If those sources don t have the answer, check online forums and newsgroups. Your service bureau can also be an excellent source for technical advice. Chances are, you re not the first person to experience the problem and someone, somewhere should have a fix for you.

>>> (4 or 1) * 2 8

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OpenType makes no distinction between Type 1 and TrueType fonts Font developers have a much easier way of porting font designs to a single format in production and mastering as well as across platforms The OpenType format is supported with font embedding and distillation Fonts eventually produced with this technology should be as reliable as you find with Type 1 and Type 42 fonts listed previously Compact Type Format: CFF is similar to the Type 1 format but offers much more compact encoding and optimization It was designed to support Type 2 fonts but can be used with other types CFF can be embedded in PDFs with the PDF Version 12 format and Acrobat 30 compatibility Fonts supporting this format are converted by Distiller during distillation to CFF/Type 2 fonts and embedded in the PDF.

Pharmaceutical drug products (eg, tablets, capsules, creams, injectables, and inhalation products) and the components in a drug product, that is, the active pharmaceutical ingredient (API, drug substance), and the inactive ingredients (excipients) should be stable in the drug product for the proposed shelf life duration of the drug product and the proposed duration of the shelf life of the individual components Shelf life (retest or expiration date) is the time period during which excipients, APIs, and drug products are expected to remain within approved shelf life speci cation, provided that they are stored under the conditions de ned on the container label Stability and storage conditions for excipients, APIs, and drug products are determined by evaluation of their quality parameters with time under the in uence of a variety of environmental factors such as temperature, humidity, and light Stability applies to chemical, physical, microbiological, therapeutic, and toxicological properties.

Note that the second example evaluates 29 (and not 54); the interpreter multiplies 4 by 6 before adding 5. Python uses operator precedence rules to decide what to do first. You can control order explicitly by using parentheses:

The US Pharmacopeia (USP) [1] de ned stability as the extent to which a product retains, within speci ed limits and throughout its period of storage and use (ie, its shelf life), the same properties and characteristics that it possessed at the time of manufacture For example, chemical stability implies that each active ingredient in a drug product retains its chemical integrity and label potency within the speci ed limits during the shelf life Physical stability is assured if the original physical properties, including appearance, palatability, uniformity, dissolution, and suspendability, are retained during the shelf life Microbiological stability is demonstrated if the sterility or resistance to microbial growth is retained according to the speci ed requirements and antimicrobial agents that are present retain effectiveness within the speci ed limits.

When viewed on-screen or printed, they are converted back to Type 1 that provides support for ATM and printing with integrity CID-keyed Fonts: This format was developed to take advantage of large character sets particularly the Asian CJK (Chinese, Japanese, and Korean) fonts The format is an extension of the Type 1 format and supports ATM and PostScript printing Kerning and spacing for these character sets are better.

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