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Developing A World Class Clinical Trial Site, Edition 2
Developing A World Class Clinical Trial Site, Edition 2
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Developing a World Class Clinical Trial Site is aimed at providing a step-by-step guide on how to create a successful clinical trial site with inbuilt tips on every aspect of the development process. It offers insight on becoming a successful clinical trial investigator, providing a comprehensive understanding of the new drug discovery and development process along with: guidance on how to get involved in a clinical trial; constitution of the study team at a site; infrastructure development; st…
  • Leidėjas:
  • Metai: 2014
  • Puslapiai: 182
  • ISBN-10: 8192227731
  • ISBN-13: 9788192227733
  • Formatas: 14 x 21.6 x 1 cm, minkšti viršeliai
  • Kalba: Anglų

Developing A World Class Clinical Trial Site, Edition 2 (el. knyga) (skaityta knyga) | knygos.lt

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Developing a World Class Clinical Trial Site is aimed at providing a step-by-step guide on how to create a successful clinical trial site with inbuilt tips on every aspect of the development process. It offers insight on becoming a successful clinical trial investigator, providing a comprehensive understanding of the new drug discovery and development process along with: guidance on how to get involved in a clinical trial; constitution of the study team at a site; infrastructure development; study initiation, conduct, and closeout; safety reporting; informed consent process; investigational product accountability and management; maintenance of source document; completion of case report forms; HIPAA privacy rules; clinical trial monitoring; and regulatory inspections. The book could serve as an effective learning resource for the clinicians who wish to become researchers.

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  • Autorius: P K Julka
  • Leidėjas:
  • Metai: 2014
  • Puslapiai: 182
  • ISBN-10: 8192227731
  • ISBN-13: 9788192227733
  • Formatas: 14 x 21.6 x 1 cm, minkšti viršeliai
  • Kalba: Anglų

Developing a World Class Clinical Trial Site is aimed at providing a step-by-step guide on how to create a successful clinical trial site with inbuilt tips on every aspect of the development process. It offers insight on becoming a successful clinical trial investigator, providing a comprehensive understanding of the new drug discovery and development process along with: guidance on how to get involved in a clinical trial; constitution of the study team at a site; infrastructure development; study initiation, conduct, and closeout; safety reporting; informed consent process; investigational product accountability and management; maintenance of source document; completion of case report forms; HIPAA privacy rules; clinical trial monitoring; and regulatory inspections. The book could serve as an effective learning resource for the clinicians who wish to become researchers.

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