Safety Pharmacology In Pharmaceutical Development : Approval And Post Marketing Surveillance / Shayne C. Gad.
Von: Gad, Shayne C.
Mitwirkende(r): Gad, Shayne C. Safety pharmacology in pharmaceutical development and approval.
Materialtyp:
BuchVerlag: Boca Raton, FL : CRC Press, c2012Auflage: 2nd ed.Beschreibung: xv, 197 P. : ill. ; 24 cm.ISBN: 9781439845677 (hardback : alk. paper).Schlagwörter: Drug Evaluation, Preclinical | Drug Approval | Product Surveillance, Postmarketing | Toxicity TestsDDC-Klassifikation: 615.704 Zusammenfassung: "This book covers the regulatory required evaluation and study of the potentially adverse pharmacological effects of new drugs, from the general regulatory requirements to the specific studies that must be done and how they are performed and interpreted. Based on more than 30 years of direct experience, the author describes tricks and practical insights for making studies work and understanding why they don't. The second edition includes current regulations (US FDA and international especially Europe and Japan) and updated test methods, interpretation, and science"--Provided by publisher.
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6october 1104 | تزويد بطلب د سيد التونسي | 615.704 G S (Regal durchstöbern) | 1 | Verfügbar |
Regale von 6october durchstöbern , Standort: 1104 , Sammlung: تزويد بطلب د سيد التونسي Regal ausblenden
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| 615.329 G A Antibiotics : | 615.58 D P Pharmacotherapy : | 615.6 D A Advances in Protein Chemistry and Structural Biology : | 615.704 G S Safety Pharmacology In Pharmaceutical Development : | 615.7045 P B Biochemical pharmacology / | 615.7045 T M Drug Interaction Facts : | 615.798 R H Handbook of anticancer pharmacokinetics and pharmacodynamics / |
سيد التونسي / كتب كلية الصيدلة
Rev. ed. of: Safety pharmacology in pharmaceutical development and approval. c2004.
Includes bibliographical references and index.
"This book covers the regulatory required evaluation and study of the potentially adverse pharmacological effects of new drugs, from the general regulatory requirements to the specific studies that must be done and how they are performed and interpreted. Based on more than 30 years of direct experience, the author describes tricks and practical insights for making studies work and understanding why they don't. The second edition includes current regulations (US FDA and international especially Europe and Japan) and updated test methods, interpretation, and science"--Provided by publisher.
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