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Books on the topic 'Standard drug'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

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1

L, Woods Adrienne, ed. PDR nurse's drug handbook: The information standard for prescription drugs and nursing considerations. 2nd ed. Delmar Learning, 2005.

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2

George, Spratto, and Woods Ardienne L, eds. PDR nurse's drug handbook: The information standard for prescription drugs and nursing considerations. 2nd ed. Thomas Delmar Learning, 2006.

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3

Resources, LLC Employers. Standard operating procedures: Non-DOT, DOT drug and alcohol management. Baker Pub., 2002.

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4

Great Britain. Department for Health. and Health Development Agency, eds. Drug education (including alcohol and tobacco): National Healthy School Standard. Health Development Agency, 2004.

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5

D, Nally Joseph, ed. Good manufacturing practices for pharmaceuticals. 6th ed. Informa Healthcare, 2007.

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6

J, Bailey C., ed. Metformin: The gold standard. John Wiley & Sons, 2007.

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7

Malawi. Ministry of Health and Population. Malawi standard treatment guidelines: MSTG 1998 ; incorporating, Malawi national drug list : MNDL 1998. 3rd ed. Malawi Government , Ministry of Health & Population, 1998.

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8

A, Bachmann Kenneth, ed. Lexi-Comp's drug interactions handbook: The new standard for drug and herbal interactions : featuring a complete guide to cytochrome P450 enzyme substrates, inducers, and inhibitors. Lexi-Comp, 2003.

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9

Jane, Ferraro Mary, and National Committee for Clinical Laboratory Standards., eds. Methods for dilution antimicrobial susceptibility tests for bacteria that grow aerobically: Approved standard. 5th ed. NCCLS, 2000.

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10

A, Bachmann Kenneth, ed. Lexi-Comp's drug interactions handbook: The new standard for drug and herbal interactions featuring a complete guide to cytochrome P450 enzyme substrates, inducers, and inhibitors. 2nd ed. Lexi-Comp, 2004.

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11

Gastl, G. Standard operating procedures for clinical trials of the CESAR Central European Society for Anticancer Drug Research - EWIV. Karger, 2003.

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12

Yu, L. X., and Bing V. Li. FDA bioequivalence standards. AAPS Press/Springer, 2014.

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13

Ethiopia) Biennial Scientific Conference on Medicines Regulation in Africa (2nd 2015 Addis Ababa. Book of abstracts: 2nd Biennial Scientific Conference on Medicines Regulation in Africa : "regulatory systems strengthening for advancing research, innovation and local pharmaceutical production in Africa", 30th November-1st December 2015, African Union Headquarters, Addis Ababa, Ethiopia. [NEPAD Planning and Coordinating Agency], 2015.

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14

AAPS Workshop on "Pharmaceutical Stability Testing to Support Global Markets" (2007 Bethesda, Md.). Pharmaceutical stability testing to support global markets. Springer, 2010.

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15

Directorate, Canada Drugs. Impurities in new drug substances. Health Protection Branch, Health and Welfare Canada, 1995.

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16

Lodola, Alberto, and Jeanne Stadler. Pharmaceutical toxicology in practice: A guide for non-clinical development. Wiley, 2011.

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17

United States. Food and Drug Administration. Office of Public Affairs., ed. FDA-approved bargain drugs: Generic products must meet high standards. 2nd ed. Dept. of Health and Human Services, Food and Drug Administration, Office of Public Affairs, 2003.

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18

Abuse, Massachusetts Supreme Judicial Court Standing Committee on Substance. Standards on substance abuse. Supreme Judicial Court, 1998.

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19

Vasilenko, Gleb, Diana Shuruhnova, and Nikolay Artem'ev. Interdepartmental standart of anti-drug preventive activities. INFRA-M Academic Publishing LLC., 2024. http://dx.doi.org/10.12737/2135823.

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The scientific and practical manual combines the results of research work carried out in 2021-2023 in order to: develop basic, uniform in content apporoaches of all interested federal executive authorities to the prevention of illicit drug use and trafficking; determining the basic requirements for such activities; establishing the role and place of specific federal executive authorities in the overall prevention system

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20

Office, General Accounting. Pesticides: Options to achieve a single regulatory standard : report to Congressional committees. The Office, 1994.

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21

Health, Malawi Ministry of, and Malawi Essential Drugs Programme, eds. Standard treatment guidelines, 1990. The Ministry, 1990.

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22

Meeting, World Health Organization Expert Committee on the Selection and Use of Essential Medicines. The selection and use of essential medicines. World Health Organization, 2003.

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23

Durivage, Mark Allen. Certified pharmaceutical GMP professional handbook. ASQ Quality Press, 2014.

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24

United States. Congress. Senate. Special Committee on Aging. Buyer beware: Public health concerns of counterfeit medicine : hearing before the Special Committee on Aging, United States Senate, One Hundred Seventh Congress, second session, Washington, DC, July 9, 2002. U.S. G.P.O., 2002.

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25

Association, American Pharmacists, ed. Compounding guide for ophthalmic preparations. American Pharmacists Association, 2013.

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26

United, Kingdom Central Council for Nursing Midwifery and Health Visiting. Standards for the administration of medicines. United Kingdom Central Council for Nursing, Midwifery and Health Visiting, 1992.

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27

Chao, Han, Davis Charles B, and Wang Binghe PhD, eds. Evaluation of drug candidates for preclinical development: Pharmacokinetics, metabolism, pharmaceutics, and toxicology. John Wiley & Sons, 2010.

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28

1948-, Gad Shayne C., ed. Safety assessment for pharmaceuticals. Van Nostrand Reinhold, 1995.

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29

Haider, Syed Imtiaz. Validation standard operating procedures: A step-by-step guide for achieving compliance in the pharmaceutical, medical device, and biotech industries. 2nd ed. Taylor & Francis, 2006.

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30

1935-, Guarino Richard A., ed. New drug approval process: Accelerating global registrations. 4th ed. M. Dekker, 2004.

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31

V, Allen Loyd, and American Pharmaceutical Association, eds. Allen's compounded formulations: The complete U.S. pharmacist collection. American Pharmaceutical Association, 2003.

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32

DSPRUD. Drug Store Management: Standard Operating Prodecures. 2006.

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33

Shaju, Shalini. Neonatal Drug Calculation Based on the Standard Concentration. Independently Published, 2019.

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34

Delmar Nurses Drug Handbook The Information Standard For Prescription Drugs And Nursing Considerations. Cengage Learning, 2011.

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35

Bulfin, Keith. Undercover [Standard Large Print 16 Pt Edition]. ReadHowYouWant.com, Limited, 2011.

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36

Nally, Joseph D. Good Manufacturing Practices for Pharmaceuticals, Sixth Edition (Drugs and the Pharmaceutical Sciences). 6th ed. Informa Healthcare, 2006.

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37

Nally, Joseph D., and Joseph D. Dally. Good Manufacturing Practices for Pharmaceuticals. Taylor & Francis Group, 2016.

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38

Model Compliant Standard Operating Procedures for Pharmaceutical Drug Manufacturers Good Laboratory Practices. F R Parker, 2000.

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39

ASHP® Injectable Drug Information™. American Society of Health-System Pharmacists, 2021. http://dx.doi.org/10.37573/9781585286850.

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Our new ASHP® Injectable Drug Information™ remains the gold standard for information on compatibility, stability, storage, and preparation of parenteral drugs. For the first time ever, ASHP® Injectable Drug Information™ is available as an eBook with new and expanded information. The 2021 edition features 18 new monographs, and nearly 200 new references for a total of over 24,000 total compatibility pairs.

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40

Csete, Joanne, Rick Lines, and Ralf Jürgens. Drug Use and Prison. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199374847.003.0012.

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This chapter discusses protections of the health-related rights of prisoners that are encoded in widely ratified human rights instruments and in guidelines for which there is broad international consensus. People who use drugs while detained or incarcerated, however, rarely enjoy the standard of care to which they are entitled, which includes HIV prevention activities and other services that are available in the community. In some countries, people accused of minor drug infractions may be detained for long periods in centers that purport to provide treatment for drug dependence but are effecti

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41

Haider, Syed Imtiaz. Validation Standard Operating Procedures. Taylor & Francis Group, 2019.

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42

Schweitzer, Stuart O., and Z. John Lu. Drug Approval Process in the United States. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780190623784.003.0013.

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The drug approval process in any country involves a balancing of conflicting social objectives: safety and access. Faster approval leads to quicker access to potentially life-saving medicine, yet could also lead to false positives or, worse, unsafe products on the market. The United States has a widely respected but stringent and rigorous review process overseen by the Food and Drug Administration. This chapter performs an in-depth analysis of the pharmaceutical regulatory approval process in the United States. Standards, guidelines, and critical milestones for basic research, animal testing,

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43

Lexi-Comp's drug interactions handbook: The new standard for drug and herbal interactions featuring a complete guide to cytochrome P450 enzyme substrates, inducers, and inhibitors. Lexi-Comp, 2004.

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44

Izzedine, Hassan, and Victor Gueutin. Drug-induced acute tubulointerstitial nephritis. Edited by Adrian Covic. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0084.

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Drug-induced acute tubulointerstitial nephritis (ATIN) is the most common aetiology of ATIN and a potentially correctable cause of acute kidney injury (AKI). An interval of 7–10 days typically exists between drug exposure and development of AKI, but this interval can be considerably shorter following re-challenge or markedly longer with certain drugs. It occurs in an idiosyncratic and non-dose-dependent manner. Antibiotics, NSAIDs, and proton pump inhibitors are the most frequently involved agents, but the list of drugs that can induce ATIN is continuously increasing. The mechanism of renal in

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45

Kawałek, Anna Grace. Problem-Solving Courts, Criminal Justice and the International Gold Standard: Reframing the English and Welsh Drug Courts. Taylor & Francis Group, 2020.

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46

Kawałek, Anna Grace. Problem-Solving Courts, Criminal Justice and the International Gold Standard: Reframing the English and Welsh Drug Courts. Taylor & Francis Group, 2020.

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47

Kawałek, Anna Grace. Problem-Solving Courts, Criminal Justice and the International Gold Standard: Reframing the English and Welsh Drug Courts. Taylor & Francis Group, 2020.

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48

Kawałek, Anna Grace. Problem-Solving Courts, Criminal Justice and the International Gold Standard: Reframing the English and Welsh Drug Courts. Taylor & Francis Group, 2020.

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49

Kawalek, Anna. Problem-Solving Courts, Criminal Justice, and the International Gold Standard: Reframing the English and Welsh Drug Courts. Routledge, Chapman & Hall, Incorporated, 2022.

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50

RU-486: Demonstrating a low standard for women's health? : hearing before the Subcommittee on Criminal Justice, Drug Policy, and Human Resources of the Committee on Government Reform, House of Representatives, One Hundred Ninth Congress, second session, May 17, 2006. U.S. G.P.O., 2007.

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