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Books on the topic 'Pharmaceutical Record'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Shepherd, Michele F. Clinical skills program: Advancing pharmaceutical care : module 1, reviewing patient medical charts. American Society of Hospital Pharmacists, 1992.

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2

Gough, Janet. Write it down: Guidance for preparing documentation that meets regulatory requirements. Interpharm Press, 2000.

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3

Gough, Janet. Write it down: Guidance for preparing effective and compliant documentation. 2nd ed. Taylor & Francis, 2005.

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4

L, Katz Laura, ed. HIPAA training: An introduction to confidentiality and privacy under HIPAA for pharma field personnel. ePharmaceuticals, 2004.

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5

United States. Congress. House. Committee on Energy and Commerce. Domestic Chemical Diversion Control Act of 1993: Report ( to accompany H.R. 3216 ... referred jointly to the Committee on Energy and Commerce and the Committee on the Judiciary) (including cost estimate of the Congressional Budget Office). U.S. G.P.O., 1993.

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6

United States. Congress. House. Committee on Energy and Commerce. Domestic Chemical Diversion Control Act of 1993: Report ( to accompany H.R. 3216 ... referred jointly to the Committee on Energy and Commerce and the Committee on the Judiciary) (including cost estimate of the Congressional Budget Office). U.S. G.P.O., 1993.

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7

Anderson, Philip O. Pharmacy informatics. Taylor & Francis, 2010.

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8

Detection and prevention of adverse drug events: Information technologies and human factors. IOS Press, 2009.

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9

Anonyma. American Druggist And Pharmaceutical Record, Volume 67. Arkose Press, 2015.

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10

Nigel, Tallis, and Arnold-Forster Kate, eds. Pharmacy history: A pictorial record : photographs from the Museum of the Royal Pharmaceutical Society of Great Britain. Pharmaceutical Press, 1991.

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11

Lesley, Richmond, Stevenson Julie, and Turton Alison, eds. The pharmaceutical industry: A guide to historical records. Ashgate, 2003.

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12

Flanigan, Jessica. Responsibility and Regulation. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190684549.003.0004.

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The case against approval requirements is even stronger than the empirical record suggests. When patients die because they knowingly and willingly used a dangerous pharmaceutical, drug manufacturers are not culpable for patients’ deaths because patients consent to the risks associated with dangerous drugs. Yet when patients die because they were prohibited from accessing a drug, those who stand in their way are morally responsible for their deaths. This argument appeals to a moral distinction between killing and letting die, which marks out particular policies, those that kill people rather th

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13

GAMP good practice guide: A risk-based approach to compliant electronic records and signatures. ISPE, 2005.

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14

(Editor), Lesley Richmond, Julie Stevenson (Editor), and Alison Turton (Editor), eds. The Pharmaceutical Industry: A Guide to Historical Records (Studies in British Business Archives). Ashgate Publishing, 2003.

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15

Gough, Janet. Write it Down: Guidance for Preparing Effective and Compliant Documentation, Second Edition. 2nd ed. Informa Healthcare, 2005.

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16

Gough, Janet. Write It Down: Guidance for Preparing Documentation that Meets Regulatory Requirements. CRC, 1999.

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17

Lopez, Orlando. Data Integrity in Pharmaceutical and Medical Devices Regulation Operations: Best Practices Guide to Electronic Records Compliance. Productivity Press, 2016.

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18

Lopez, Orlando. Data Integrity in Pharmaceutical and Medical Devices Regulation Operations: Best Practices Guide to Electronic Records Compliance. Productivity Press, 2016.

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19

Goldman, Stephen Robert. Handbook of Computer and Computerized System Validation for the Pharmaceutical Industry (1stbooks Library (Series).). 1st Books Library, 2003.

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20

Hogue, Michael D. The Pharmacist's Guide to Compensation for Patient-Care Services. APhA Publications, 2002.

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21

Birks, David, and Thomas Douglas, eds. Treatment for Crime. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198758617.001.0001.

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Crime-preventing neurointerventions (CPNs) are increasingly being used or advocated for crime prevention. There is increasing use of testosterone-lowering agents to prevent recidivism in sexual offenders, and strong political and scientific interest in developing pharmaceutical treatments for psychopathy and anti-social behaviour. Recent developments suggest that we may ultimately have at our disposal a range of drugs capable of suppressing violent aggression, and it is not difficult to imagine possible applications of such drugs in crime prevention. But should neurointerventions be used in cr

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22

Farb, Daniel. GMP Training Package: The FDA Regulations on Part 11, Electronic Records and Electronic Signatures, for Pharmaceutical, Medical Device, Food, and Cosmetics Manufacturing. University Of Health Care, 2004.

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23

Farb, Daniel. Part 11 and Computer Validation Library Edition: The FDA Regulations on Part 11, Electronic Records and Electronic Signatures, for Pharmaceutical, Medical Device, Food, and Cosmetics Manufacturing. University Of Health Care, 2004.

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24

Domestic Chemical Diversion Control Act of 1993: Report ( to accompany H.R. 3216 ... referred jointly to the Committee on Energy and Commerce and the Committee on the Judiciary) (including cost estimate of the Congressional Budget Office). U.S. G.P.O., 1993.

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25

Gordon, Bruce, and Daniel Farb. Agent GXP FDA Part 11 Guidebook: The FDA Regulations on Part 11, Electronic Records and Electronic Signatures, For Pharmaceutical, Medical Device, Food, ... Trials and GCP (Good Clinical Practices). UniversityOfHealthCare, 2005.

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26

Part 11 and Computer Validation Manual and CD, The FDA Regulations on Part 11, Electronic Records and Electronic Signatures, For Pharmaceutical, Medical ... Emphasis on Computer System Validation a. UniversityOfHealthCare, 2003.

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27

Gordon, Bruce, and Daniel Farb. Agent GXP FDA Part 11 Manual and CD, The FDA Regulations on Part 11, Electronic Records and Electronic Signatures, For Pharmaceutical, Medical Device, ... Trials and GCP (Good Clinical Practices). UniversityOfHealthCare, 2003.

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28

Farb, Daniel. Agent GXP FDA Part 11 Five Users: The FDA Regulations on Part 11, Electronic Records and Electronic Signatures, for Pharmaceutical, Medical Device, Food, ... Trials and GCP (Good Clinical Practices). UniversityOfHealthCare, 2005.

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29

Gordon, Bruce, and Daniel Farb. GMP Training Package Manual and CD, The FDA Regulations on Part 11, Electronic Records and Electronic Signatures, For Pharmaceutical, Medical Device, Food, ... System Validation and Part 11, Covering FD. UniversityOfHealthCare, 2003.

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30

Bourne, Philip E., Philip O. Anderson, and Susan M. McGuinness. Pharmacy Informatics. CRC, 2009.

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