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Michael Brooks, Thanks But No Thanks, New Scientist, Oct 6, 2001, at 33 67 Robert A Freitas Jr, Foresight Inst, What Could Go Wrong During a Nanomedical Procedure, in Nanotech FAQ, 1998, at http://wwwforesightorg/Nanomedicine/NanoMedFAQhtml#FAQ18 68 Lewin Group, supra note 11, at 26 (citing the FDA FY 2001 Congressional Budget Request) 69 Henney, supra note 1 70 Kathryn Zoon, The Impact of New Biotechnology on the Regulation of Drugs and Biologics, 41 Food Drug Cosm LJ 429, 430 (Oct 1986) 71 David T Bonk, FDA Regulation of Biotechnology, 43 Food Drug Cosm LJ 67, 77 (Jan 1988) 72 The first Points To Consider concerned Interferon, products derived from rDNA technology, monoclonal antibody products, and cell lines used to produce biologicals See Zoon, supra note 70, at 431 73.

I keep threatening to take some vacation time to visit the reading room of the FCC in Washington some time and look this stuff up, but I really can t afford the trip (see comment on Right-To-Work state above) Since I cover a number of states in my job, I get to look at the listings of a number of major LECs.

If you want to have any hope of really understanding the memory architecture of Windows 95, there's simply no way to avoid understanding memory paging on the Intel 80386 class of CPUs. Although the technique of memory paging far predates the 80386, we're interested only in how Windows 95 uses paging on the 80386, so I'll speak in 80386-specific terms. If you already know paging cold, you can skip this section. If memory paging is mysterious to you or if you need a quick refresher, read on.

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For example, in 1991, the FDA published a Points To Consider document on human somatic cell and gene therapies In 1995, the FDA published a Points to Consider document on therapeutic products derived from transgenic animals Martha J Carter, The Ability of Current Biologics Law to Accommodate Emerging Technologies, 51 Food Drug LJ 375, 376 (1996) 74 Id 75 55 Fed Reg 12, 284 (1990) 76 55 Fed Reg 12,284 (1990) 77 Sandra H Cuttler, The Food and Drug Administration s Regulation of Genetically Engineered Human Drugs, 1 The J Pharm & Law 191, 210 (1992); see also David Hanson, Pharmaceutical Industry Optimistic About Improvements at FDA, Chem & Eng News, Jan 27, 1992, at 28-29 78 FDA Dumps Office of Biotechnology: Miller to Stanford as Visiting Scholar, Biotechnology Newswatch, Jan.

17, 1994, at 13 ( Abolishing the office is no signal that biotechnology is less important , an FDA spokesman said The agency looks at that office as one established when biotechnology was an emerging technology, he said It is no longer emerging , the spokesman pointed out These days, most decisions regarding biotechnology are being made at the Center for Biologics Evaluation and Research rather than at the commissioner s level, he said ) 79 Larry Thompson, Science at FDA: The Key to Making the Right Decision, FDA Consumer Magazine, March-April 2000, at http://wwwfdagov/fdac/ features/2000/200_scihtml..

Verizon will have Verizon Wireless listings for every hamlet and burg in the nation, but try to find a number for residential land-line service that an out-ofstate caller can ring up to see about the problem with Aunt Minnie s account back home, and I m up against the tariff asking Do you know the name of the phone company in that area Even when I break down and suggest that Verizon is the primary local carrier in Boston, or Ameritech in Chicago (hoping that this isn t one of the calls being monitored for Quality Assurance ), just what number am I supposed to supply Deregulation began in 1986 with the Modified Final Judgment.

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