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Pharmaceutical Medicine.
The breadth of the pharmaceutical medicine can be daunting, but this book is designed to navigate a path through the speciality. Providing a broad overview of all topics relevant to the discipline of pharmaceutical medicine, it gives you the facts fast, in a user-friendly format, without having to d...
| Clasificación: | Libro Electrónico |
|---|---|
| Autor principal: | |
| Otros Autores: | , |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
[Oxford] :
Oxford University Press,
2013.
|
| Colección: | Oxford specialist handbooks.
|
| Temas: | |
| Acceso en línea: | Texto completo |
MARC
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| 050 | 4 | |a RS122.95 .K384 2013 | |
| 072 | 7 | |a MED |x 023000 |2 bisacsh | |
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| 082 | 0 | 4 | |a 615.1 |
| 049 | |a UAMI | ||
| 100 | 1 | |a Kilcoyne, Adrian. | |
| 245 | 1 | 0 | |a Pharmaceutical Medicine. |
| 246 | 3 | |a Oxford Specialist Handbooks | |
| 264 | 1 | |a [Oxford] : |b Oxford University Press, |c 2013. | |
| 300 | |a 1 online resource (473 pages) | ||
| 336 | |a text |b txt |2 rdacontent | ||
| 337 | |a computer |b c |2 rdamedia | ||
| 338 | |a online resource |b cr |2 rdacarrier | ||
| 490 | 1 | |a Oxford Specialist Handbooks | |
| 588 | 0 | |a Print version record. | |
| 504 | |a Includes bibliographical references and index. | ||
| 505 | 0 | |a Cover; Contents; Preface; Contributors; Abbreviations; Section 1: Discovery of new medicines; 1.1 Intellectual property in discovery; 1.2 Targeted drug discovery: receptor-based approaches; 1.3 In vitro and in vivo testing of new compounds; 1.4 Lead optimization; 1.5 Natural products and herbal medicines; Section 2: Medicines regulation; 2.1 General principles of medicines regulation; 2.2 Medicines regulation in the UK; 2.3 Medicines regulation in the EU; 2.4 The European Medicines Agency and Heads of Medicines Agencies. | |
| 505 | 8 | |a 2.5 The European Directorate for the Quality of Medicines and HealthCare, European Pharmacopoeia, and British Pharmacopoeia2.6 The Food and Drug Administration; 2.7 Health Canada; 2.8 Medsafe and the Therapeutic Goods Administration; 2.9 Medicines regulation in Japan; 2.10 Medicines regulation in China; 2.11 Medical device regulation; 2.12 Clinical trials regulation; 2.13 Good clinical practice; 2.14 Good laboratory practice and good clinical laboratory practice; 2.15 Good manufacturing practice; 2.16 The Ethics Committee (EU); 2.17 The Institutional Review Board (US). | |
| 505 | 8 | |a 2.18 Marketing authorization applications and updating and maintaining licences2.19 The International Conference on Harmonisation; 2.20 Common technical document; 2.21 Medicinal product information in the European Union; 2.22 Summary of product characteristics; 2.23 Orphan drugs; 2.24 Paediatric investigational plans; 2.25 Regulatory requirements for pharmacovigilance; 2.26 Overview of reporting of adverse drug reactions; 2.27 Non-prescription drugs; 2.28 Provision of unlicensed medicines; 2.29 Reclassification of medicines; 2.30 Parallel imports; Section 3: Clinical pharmacology. | |
| 505 | 8 | |a 3.1 Absorption, distribution, metabolism, and excretion3.2 Volume of distribution, clearance, half-life; 3.3 Pre-clinical aspects of pharmacokinetics; 3.4 Non-clinical data; 3.5 Clinical aspects of pharmacokinetics; 3.6 Dose-response relationship; 3.7 Proof of concept studies; 3.8 Reproductive toxicity studies; 3.9 Immunotoxicity testing; 3.10 Carcinogenicity; 3.11 Genotoxicity testing; 3.12 Local tolerance; 3.13 Acute toxicity; 3.14 Studies: objectives, design, conduct, and analysis; 3.15 Populations for exploratory studies and planning of exploratory studies; 3.16 Pharmacodynamic endpoints. | |
| 505 | 8 | |a 3.17 Bioavailability and bioequivalence3.18 Evaluation of safety and tolerability; 3.19 Hypersensitivity reactions; 3.20 Drug-drug interactions; 3.21 Ethics in research: basic principles, Declaration of Helsinki, and Council for International Organizations of Medical Sciences; 3.22 Disease models; 3.23 Biomarkers; 3.24 Pharmacogenetics; 3.25 Population pharmacokinetics; 3.26 Small molecules and biologicals: safety and pharmacology requirements; Section 4: Clinical development; 4.1 Requirements for licensing a new medicinal product; 4.2 Regulatory guidance. | |
| 500 | |a 4.3 General principles of clinical trial protocols. | ||
| 520 | |a The breadth of the pharmaceutical medicine can be daunting, but this book is designed to navigate a path through the speciality. Providing a broad overview of all topics relevant to the discipline of pharmaceutical medicine, it gives you the facts fast, in a user-friendly format, without having to dive through page upon page of dense text. With 136 chapters spread across 8 sections, the text offers a thorough grounding in issues ranging from medicines regulation to clinical trial design and data management. This makes it a useful revision aid for exams as well as giving you a taster of areas o. | ||
| 546 | |a English. | ||
| 588 | 0 | |a Online resource; title from home page (viewed on July 8, 2013). | |
| 590 | |a eBooks on EBSCOhost |b EBSCO eBook Subscription Academic Collection - Worldwide | ||
| 650 | 0 | |a Clinical pharmacology. | |
| 650 | 0 | |a Drug development. | |
| 650 | 0 | |a Medical personnel. | |
| 650 | 0 | |a Therapeutics. | |
| 650 | 0 | |a Drugs. | |
| 650 | 0 | |a Chemotherapy. | |
| 650 | 0 | |a Pharmacy. | |
| 650 | 2 | |a Chemicals and Drugs | |
| 650 | 2 | |a Health Occupations | |
| 650 | 2 | |a Therapeutics | |
| 650 | 2 | |a Analytical, Diagnostic and Therapeutic Techniques and Equipment | |
| 650 | 2 | |a Disciplines and Occupations | |
| 650 | 2 | |a Pharmaceutical Preparations | |
| 650 | 2 | |a Drug Therapy | |
| 650 | 2 | |a Pharmacy | |
| 650 | 2 | |a Pharmacology, Clinical | |
| 650 | 6 | |a Pharmacologie clinique. | |
| 650 | 6 | |a Médicaments |x Développement. | |
| 650 | 6 | |a Personnel médical. | |
| 650 | 6 | |a Thérapeutique. | |
| 650 | 6 | |a Médicaments. | |
| 650 | 6 | |a Chimiothérapie. | |
| 650 | 6 | |a Pharmacie. | |
| 650 | 7 | |a pharmacies (health facilities ) |2 aat | |
| 650 | 7 | |a treating (health care function) |2 aat | |
| 650 | 7 | |a pharmacy (discipline) |2 aat | |
| 650 | 7 | |a MEDICAL |x Drug Guides. |2 bisacsh | |
| 650 | 7 | |a MEDICAL |x Nursing |x Pharmacology. |2 bisacsh | |
| 650 | 7 | |a MEDICAL |x Pharmacology. |2 bisacsh | |
| 650 | 7 | |a MEDICAL |x Pharmacy. |2 bisacsh | |
| 650 | 7 | |a Therapeutics |2 fast | |
| 650 | 7 | |a Pharmacy |2 fast | |
| 650 | 7 | |a Medical personnel |2 fast | |
| 650 | 7 | |a Drugs |2 fast | |
| 650 | 7 | |a Chemotherapy |2 fast | |
| 650 | 7 | |a Clinical pharmacology |2 fast | |
| 650 | 7 | |a Drug development |2 fast | |
| 700 | 1 | |a Ambery, Phil. | |
| 700 | 1 | |a O'Connor, Daniel. | |
| 776 | 0 | 8 | |i Print version: |t Pharmaceutical medicine |z 9780199609147 |w (OCoLC)825557405 |
| 830 | 0 | |a Oxford specialist handbooks. | |
| 856 | 4 | 0 | |u https://ebsco.uam.elogim.com/login.aspx?direct=true&scope=site&db=nlebk&AN=615422 |z Texto completo |
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