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      1. Medicin
      2. Andra medicinska specialiteter
      3. Farmakologi

      Safety Evaluation of Pharmaceuticals and Medical Devices

      International Regulatory Guidelines

      AvShayne C. Gad

      Inbunden, Engelska, 2010

      1 686 kr

      Beställningsvara. Skickas inom 10-15 vardagar. Fri frakt över 249 kr.

      Fler format och utgåvor

      E-bok

      2 105 kr

      Häftad

      1 686 kr

      Beskrivning

      The inspiration for this text was the 1988 volume by Alder and Zbinden, written before the ICH harmonization process for drug safety evaluation (or its ISO analog for device biocompatibility evaluation) had been initiated or come to force. Since then, much has changed in both the world and practice of medicine and the regulation of drugs. The intent of this volume is to provide similar guidance as to what nonclinical safety assessment tests need to be performed to move a drug into man, through development and to market approved (this intent was subsequently extended to cover the closely related medical device biotechnology, and combination product fields) in a concise, abbreviated manner for all the major world market countries.

      Produktinformation

      • Utgivningsdatum:2010-10-27
      • Mått:155 x 235 x 18 mm
      • Vikt:352 g
      • Format:Inbunden
      • Språk:Engelska
      • Antal sidor:126
      • Förlag:Springer-Verlag New York Inc.
      • ISBN:9781441974488

      Utforska kategorier

      • Farmakologi inom Medicin
      • Kemi inom Naturvetenskap och teknik
      • Apotek och farmaceuter inom Medicin

      Mer om författaren

      Shayne C. Gad, B.S. (Whittier College, Chemistry and Biology, 1970) and Ph.D. in Pharmacology/Toxicology (Texas, 1977) DABT, ATS, is the principal of Gad Consulting Services, a seventeen year old consulting firm with six employees and more than 450 clients (including 120 pharmaceutical companies in the US and 50 overseas). Prior to this, he served in director-level and above positions at Searle, Synergen and Becton Dickinson. He has published 39 books and more than 350 chapters, articles and abstracts in the fields of toxicology, statistics, pharmacology, drug development and safety assessment. He has more than 33 years of broad based experience in toxicology, drug and device development, statistics and risk assessment. He has specific expertise in neurotoxicology, in vitro methods, cardiovascular toxicology, inhalation toxicology, immunotoxicology, and genotoxicology. Past President of the American College of Toxicology, the Roundtable of Toxicology Consultants and three of SOT,s specialty sections, and recipient of the American College of Toxicology Lifetime Contribution Award. He has direct involvement in the preparation of INDs (90 successfully to date), NDA, PLA, ANDA, 510(k), IDE, CTD, clinical data bases for phase 1 and 2 studies, and PMAs. He has consulted for FDA, EPA and NIH, and has trained reviewers and been an expert witness for FDA. He has also conducted the triennial toxicology salary survey as a service to the profession for the last 19 years.

      Innehållsförteckning

      • Preface.- Introduction to Safety Assessment in Drug and Medical Device Development.- Drugs: The General Case.- Ind Enabling Toxicology Programs.- Nonclinical Safety Evaluation Studies Conducted To Support Continued Clinical Development.- Supporting Marketing Applications.- Special Therapeutic Category And Route Of Administration Cases.- Device Safety Evaluation.- Appendix A.- INDEX.
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