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Medical supplies -- United States -- Classification

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• Medical supplies -- United States
• Classification

• Drugs -- United States -- Classification
• Medical instruments and apparatus -- United States -- Classification

• Classification names for medical devices and in vitro diagnostic products (U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1991), by Center for Devices and Radiological Health (U.S.). Office of Compliance (page images at HathiTrust)

• Drug registration and listing instruction booklet. (U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Drug Evaluation and Research, Product Information Management Branch, 1996), by Center for Drug Evaluation and Research (U.S.). Product Information Management Branch (page images at HathiTrust)

• DRLS, drug establishment registration and drug listing instruction booklet. (U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Drug Evaluation and Research, Drug Listing Branch, 1991), by Center for Drug Evaluation and Research (U.S.). Drug Listing Branch (page images at HathiTrust)

• Classification names for medical devices and in vitro diagnostic products (U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1991), by Center for Devices and Radiological Health (U.S.). Office of Compliance (page images at HathiTrust)

Items below (if any) are from related and broader terms.

• Phase V of a comparative study of VA and private sector procurement, contracting and distribution of medical supplies and non-perishable subsistence (Veterans Administration, 1986), by Coopers & Lybrand and United States. Veterans Administration (page images at HathiTrust)
• Army medical supply issues: Operation Desert Storm (The Office ;, 1993), by United States General Accounting Office and United States. Congress. Senate. Committee on Governmental Affairs. Subcommittee on Oversight of Government Management (page images at HathiTrust)
• Use of revised "inherent reasonableness" process generally appropriate (The Office, 2000), by United States General Accounting Office (page images at HathiTrust)

• HHS SSC Medical supply catalog (The Center, 1996), by Health and Human Services Supply Service Center (U.S.) (page images at HathiTrust)
• Federal supply catalog. Section VI. Nondepot items : VA medical centers stocked items. (Dept. of Veterans Affairs, Office of Acquisition and Materiel Management, 1991), by United States. Dept. of Veterans Affairs. Office of Acquisition and Materiel Management (page images at HathiTrust)
• Medical supply catalog. (U.S. Dept. of Health, Education, and Welfare, Public Health Service, Medical Supply Depot., in the 20th century), by United States. Public Health Service. Medical Supply Depot and United States. Health Resources and Services Administration. Supply Service Center (page images at HathiTrust)

• Excessive payments for medical supplies continue despite improvements (The Office ;, 1995), by United States General Accounting Office and Health and Human Services United States. Congress. Senate. Committee on Appropriations. Subcommittee on Departments of Labor (page images at HathiTrust)
• Department of Veterans Affairs pharmacy program with emphasis on OTC drugs, medical supplies, and dietary supplements : hearing before the Subcommittee on Hospitals and Health Care of the Committee on Veterans' Affairs, House of Representatives, One Hundred Fourth Congress, second session, June 11, 1996. (U.S. G.P.O. :, 1996), by United States. Congress. House. Committee on Veterans' Affairs. Subcommittee on Hospitals and Health Care (page images at HathiTrust)
• Problems affecting HCFA's ability to set appropriate reimbursement rates for medical equipment and supplies (The Office ;, 1997), by Education United States. General Accounting Office. Health (page images at HathiTrust)

• U.S. Public Health Service inventory of storage locations : pre-positioned medical supplies and equipment (The Dept., 1984), by United States. Office of Emergency Preparedness (page images at HathiTrust)

• Managing the risks from medical product use : creating a risk management framework : report to the FDA Commissioner from the Task Force on Risk Management. (U.S. Dept. of Health and Human Services, Food and Drug Administration, 1999), by United States. Food and Drug Administration. Task Force on Risk Management and United States Food and Drug Administration (page images at HathiTrust)
• Strategies to increase information on comparative clinical effectiveness (U.S. G.P.O. :, 2009), by United States. Congress. House. Committee on Ways and Means. Subcommittee on Health (page images at HathiTrust)
• Managing the risks from medical product use : creating a risk management framework : report to the FDA Commissioner from the Task Force on Risk Management : executive summary. (U.S. Dept. of Health and Human Services, Food and Drug Administration, 1999), by United States. Food and Drug Administration. Task Force on Risk Management (page images at HathiTrust)

• Combating terrorism : management of medical supplies : hearing before the Subcommittee on National Security, Veterans Affairs, and International Relations of the Committee on Government Reform, House of Representatives, One Hundred Seventh Congress, first session, May 1, 2001. (U.S. G.P.O. :, 2001), by Veterans Affairs United States. Congress. House. Committee on Government Reform. Subcommittee on National Security (page images at HathiTrust)
• Combating terrorism : management of medical supplies : hearing before the Subcommittee on National Security, Veterans Affairs, and International Relations of the Committee on Government Reform, House of Representatives, One Hundred Sixth Congress, second session, March 8, 2000. (U.S. G.P.O. :, 2000), by Veterans Affairs United States. Congress. House. Committee on Government Reform. Subcommittee on National Security (page images at HathiTrust)

• Safe and affordable biotech drugs : the need for a generic pathway : hearing before the Committee on Oversight and Government Reform, House of Representatives, One Hundred Tenth Congress, first session, March 26, 2007. (U.S. G.P.O. :, 2008), by United States House Committee on Oversight and Government Reform (page images at HathiTrust)
• Assessing the impact of a safe and equitable biosimilar policy in the United States : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Tenth Congress, first session, May 2, 2007. (U.S. G.P.O. :, 2008), by United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health (page images at HathiTrust)
• The Right choice : minority college & university program. (U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Biologics Evaluation and Research, 1991), by Center for Biologics Evaluation and Research (U.S.) (page images at HathiTrust)

• Drugs in perspective (National Institute on Drug Abuse, Division of Resource Development, Manpower and Training Branch :, 1979), by National Institute on Drug Abuse. Manpower and Training Branch, Lonnie E. Mitchell, William E. Link, and National Drug Abuse Center (U.S.) (page images at HathiTrust)
• Drugs in travelers' kit. (Center for Disease Control, 1986), by Centers for Disease Control (U.S.) (page images at HathiTrust)
• Guideline for the format and content of the summary for new drug and antibiotic applications. (Center for Drugs and Biologics, Food and Drug Administration, Dept. of Health and Human Services, 1987), by Center for Drugs and Biologics (U.S.) (page images at HathiTrust)
• Guideline on formatting, assembling, and submitting new drug and antibiotic applications. (Center for Drugs and Biologics, Food and Drug Administration, Dept. of Health and Human Services, 1987), by Center for Drugs and Biologics (U.S.) (page images at HathiTrust)
• Guideline for submitting supporting documentation in drug applications for the manufacture of drug substances (U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, 1987), by Center for Drugs and Biologics (U.S.) (page images at HathiTrust)
• Guideline for submitting documentation for the manufacture of and controls for drug products. (Center for Drugs and Biologics, Food and Drug Administration, Dept. of Health and Human Services, 1987), by Center for Drugs and Biologics (U.S.) (page images at HathiTrust)
• Coverage of prescription drugs under Medicare hearing before the Subcommittee on Health of the Committee on Finance, United States Senate, One Hundredth Congress, first session, June 18, 1987. (U.S. G.P.O., 1988), by United States. Congress. Senate. Committee on Finance. Subcommittee on Health (page images at HathiTrust)
• The Food and Drug Administration's process for approving new drugs : report (U.S. G.P.O. :, 1980), by Research United States. Congress. House. Committee on Science and Technology. Subcommittee on Science (page images at HathiTrust)
• Funding implications of new combination therapies for federal and state programs (The Office, 1998), by United States General Accounting Office and Health and Human Services United States. Congress. Senate. Committee on Appropriations. Subcommittee on Departments of Labor (page images at HathiTrust)
• An FDA consumer memo. (Dept. of Health, Education, and Welfare, Public Health Service, Food and Drug Administration, Office of Public Affairs, 1979), by United States. Food and Drug Administration. Office of Public Affairs (page images at HathiTrust)
• Further investigation of look-alike drugs : hearing before the Select Committee on Narcotics Abuse and Control, House of Representatives, Ninety-seventh Congress, second session, August 12, 1982. (U.S. G.P.O., 1983), by United States. Congress. House. Select Committee on Narcotics Abuse and Control (page images at HathiTrust)
• Federal drug interdiction efforts need strong central oversight : report to the Congress (U.S. General Accounting Office ;, 1983), by United States General Accounting Office (page images at HathiTrust)
• Criminal penalty for robbery of controlled substances : hearing before the Subcommittee on Crime of the Committee on the Judiciary, House of Representatives, Ninety-eighth Congress, first session ... April 7, 1983. (U.S. G.P.O., 1984), by United States. Congress. House. Committee on the Judiciary. Subcommittee on Crime (page images at HathiTrust)
• Spectrophotometric determination of heroine and quinine ... (Govt. Print. Off.], 1955), by United States Internal Revenue Service (page images at HathiTrust)
• Drug regulation reform act of 1978. (U.S. Govt. Print. Off., 1978), by United States Department of Health, Education, and Welfare (page images at HathiTrust)
• Milestones in the war against the narcotic peril / extension of remarks of Walter F. Lineberger of California, in the House of Representatives, Wednesday, February 18, 1925. (G.P.O. ;, 1925), by Water Franklin Lineberger (page images at HathiTrust)
• Uniform narcotic drug act drafted by the National Conference of Commissioners on Uniform State Laws, and by it approved and recommended for enactment in all the states at its forty-second annual conference at Washington, D.C., October 4-10, 1932 ... ([Chicago], 1932), by National Conference of Commissioners on Uniform State Laws (page images at HathiTrust; US access only)
• Report on doctor-owned drug enterprises ... (U.S. Govt. Print. Off.?, 1966), by United States House Committee on the Judiciary and United States Food and Drug Administration (page images at HathiTrust)
• Guidelines for the time frame applicable to the review and approval of new drug applications and antibiotic applications. (Datapharm Information Services, Division of Interpharm Press, 1985), by Center for Drugs and Biologics (U.S.) and United States Food and Drug Administration (page images at HathiTrust)
• Guideline for submitting documentation for the stability of human drugs and biologics. (Datapharm Information Services, Division of Interpharm Press, 1987), by Center for Drugs and Biologics (U.S.) and United States Food and Drug Administration (page images at HathiTrust)

• Medical technology and the health care system : a study of the diffusion of equipment-embodied technology : a report (National Academy of Sciences, 1979), by Committee on Technology and Health Care (U.S.), National Academy of Sciences (U.S.), and National Science Foundation (U.S.) (page images at HathiTrust)
• VA medical program fire and safety codes in residential care homes, income limits of veterans receiving domiciliary care, and VA medical procurement program : hearing before the Subcommittee on Oversight and Investigations of the Committee on Veterans Affairs, House of Representatives, Ninety-seventh Congress, first session, June 9, 1981. (U.S. G.P.O., 1981), by United States. Congress. House. Committee on Veterans' Affairs. Subcommittee on Oversight and Investigations (page images at HathiTrust)
• Medical device establishment registration : information and instructions (U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1987), by Center for Devices and Radiological Health (U.S.). Office of Compliance and Surveillance (page images at HathiTrust)
• Durable medical equipment : hearing before a subcommittee of the Committee on Appropriations, United States Senate, One Hundred Third Congress, second session, special hearing. (U.S. G.P.O. :, 1995), by Health and Human Services United States. Congress. Senate. Committee on Appropriations. Subcommittee on Departments of Labor (page images at HathiTrust)
• A consumer's perspective on medical devices : hearing before the Subcommittee on Oversight and Investigations of the Committee on Commerce, House of Representatives, One Hundred Fourth Congress, first session, March 30, 1995. (U.S. G.P.O. :, 1995), by United States House Committee on Commerce, Subcommittee on Oversight and Investigations (page images at HathiTrust)
• Medical devices : early warning of problems is hampered by severe underreporting : report to the chairman, Committee on Governmental Affairs, United States Senate. (U.S. General Accounting Office, 1986), by United States General Accounting Office and United States Senate Committee on Governmental Affairs (page images at HathiTrust)
• How to : instructions for the DRS Scientific Equipment Rental Program. (National Institutes of Health, 1987), by National Institutes of Health (U.S.). Biomedical Engineering and Instrumentation Branch (page images at HathiTrust)
• Product liability reform : hearings before the Subcommittee on Telecommunications, Trade, and Consumer Protection of the Committee on Commerce, House of Representatives, One Hundred Fifth Congress, first session, April 8, 1997 .... (U.S. G.P.O. :, 1997), by Trade United States. Congress. House. Committee on Commerce. Subcommittee on Telecommunications (page images at HathiTrust)
• Fiscal year 1991 reconciliation issues relating to durable medical equipment, clinical laboratory services, and other issues under the Medicare Program : hearing before the Subcommittee on Health of the Committee on Ways and Means, House of Representatives, One Hundred First Congress, second session, May 22, 1990. (U.S. G.P.O. :, 1990), by United States. Congress. House. Committee on Ways and Means. Subcommittee on Health (page images at HathiTrust)
• Aviation Medical Assistance Act of 1998 : report (to accompany H.R. 2843) (including cost estimate of the Congressional Budget Office). (U.S. G.P.O., 1998), by United States. Congress. House. Committee on Transportation and Infrastructure (page images at HathiTrust)
• Applications of space technology for the elderly and handicapped : joint hearings before the Select Committee on Aging and the Committee on Science and Technology, U.S. House of Representatives, Ninety-sixth Congress, first session, July 19 and 20, 1979. (U.S. Govt. Print. Off. : for sale by the Supt. of Docs., U.S. Govt. Print. Off., 1979), by United States Select Committee on Aging and United States House Committee on Science and Technology (page images at HathiTrust)
• Do cellular and other wireless devices interfere with sensitive medical equipment? : hearing before the Information, Justice, Transportation, and Agriculture Subcommittee of the Committee on Government Operations, House of Representatives, One Hundred Third Congress, second session, October 5, 1994. (U.S. G.P.O. :, 1997), by Justice United States. Congress. House. Committee on Government Operations. Information (page images at HathiTrust)
• Consolidating procurements of medical equipment could save money : report (The Office, 1985), by United States General Accounting Office (page images at HathiTrust)
• Managing your Hickman catheter (Clinical Center Communications, National Institutes of Health, 1988), by Eileen Parinisi and National Institutes of Health (U.S.). Office of Clinical Center Communications (page images at HathiTrust)
• An Act to Direct the Administrator of the Federal Aviation Administration to Reevaluate the Equipment in Medical Kits Carried on, and to Make a Decision Regarding Requiring Automatic External Defibrillators to Be Carried on, Aircraft Operated by Air Carriers, and for Other Purposes. (U.S. G.P.O. :, 1998), by United States (page images at HathiTrust)
• Investigational device exemptions : regulatory requirements for medical devices (U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, National Center for Devices and Radiological Health, 1983), by National Center for Devices and Radiological Health (U.S.). Office of Small Manufacturers Assistance (page images at HathiTrust)
• Medical device reprocessing (Washington, D.C. : The Office, [2000], 2000), by United States General Accounting Office (page images at HathiTrust)

More items available under broader and related terms at left.