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- Author: P K Julka
- Publisher: Cr Books Pvt. Ltd.
- Year: 2014
- Pages: 182
- ISBN-10: 8192227731
- ISBN-13: 9788192227733
- Format: 14 x 21.6 x 1 cm, minkšti viršeliai
- Language: English
- SAVE -10% with code: EXTRA
Developing A World Class Clinical Trial Site, Edition 2 (e-book) (used book) | bookbook.eu
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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.
EXTRA 10 % discount with code: EXTRA
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- Author: P K Julka
- Publisher: Cr Books Pvt. Ltd.
- Year: 2014
- Pages: 182
- ISBN-10: 8192227731
- ISBN-13: 9788192227733
- Format: 14 x 21.6 x 1 cm, minkšti viršeliai
- Language: English English
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.
Reviews