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They are very similar to (5.22) and (5.23). There is one important difference, though. Unlike P and q in (5.25) and (5.26), Bj and Vj in (5.22) and (5.23) are complex. This is not a big problem, however, because as we have shown in 2, with a few minor adjustments we can use the Hamiltonian formalism with complex canonical coordinates. Let us discuss this in a bit more detail here than we did there. Consider a complex version of the equations of motion (5.25) and (5.26):

Q=-,

Developing Estimates Customizing estimates Creating multiple estimates for a single customer Creating an Invoice from an Estimate Creating a progress invoice from an estimate Determining whether invoices have been created Checking Your Actual Job Cost against the Estimate Tracking Employee Time QuickBooks Pro options for tracking time Two ways to track time Entering single activities Using the internal stopwatch feature Filling out weekly timesheets Using the QuickBooks Pro Timer Overview: Using Timer for the rst time Exporting lists for Timer from QuickBooks Pro Setting up the Timer le and importing information Charging Billable Time and Costs to Invoices Viewing Time-Tracking Reports Working in Multi-User Mode Switching to multi-user mode Setting up new users Summary 357 359 360 361 361 364 365 366 366 367 368 369 369 371 371 372 372 373 374 375 375 376 376.

P=-mw Q-F,

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The Orphan Drug Act is designed to encourage the development of drugs to serve mar kets of fewer than 200,000 patients It provides a seven-year period of market exclusivity and a 50 percent tax credit for clinical research ex penses involved in developing the drug The Prescription Drug Marketing Act was enacted in 1988 to limit the diversion of prescription drugs into a secondary gray market Another major piece of legislation affecting the pharmaceutical industry is the FDA Modernization Act of 1997, which streamlined many of the processes used by the FDA, and reduced and sim pli ed many regulatory obligations of pharmaceutical manufacturers The Health Insurance Portability and Accountability Act (HIPAA), in troduced earlier in this chapter, was enacted by the Department of Health and Human Services (HHS) in part to ensure the privacy of patients who take part in clinical trials.

(5.27)

I know a wholesaler of novelty items who ordered several thousand toy frogs The frogs were supposed to make an adorable croaking sound but instead made a sickly sort of belching noise The buyer argued that these were defective goods The seller claimed they were just ne they made a noise on cue Obviously, the forms of both parties were silent as to the tenor and pitch of the simulated frog croak What does the UCC have to say about a situation like this The UCC provides that a buyer has the right to inspect the goods and reject nonconforming goods within a reasonable period of time But the buyer cannot reject the shipment of goods if he has already accepted the goods.

(5.28)

where F is a driving force (independent of Q, P). These two complex equations actually contain four equations of motion for four real variables. Let us define these four real variables in the following way:

HIPAA requires pharmaceutical companies to follow stringent security practices to prevent patient data from being ac cessed by those without access privileges In addition to the Food and Drug Administration, the US Patent and Trademark Of ce (USPTO) is a major constituent of the legal-regulatory infrastructure of the pharmaceutical industry The USPTO establishes the limits of the temporary monopoly granted pharmaceutical companies by virtue of drug patents and other intellectual property protection The role of the US Patent and Trademark Of ce in protecting intellectual prop erty, including the formulation of drugs, is discussed in more detail later in this chapter..

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