Becoming a successful clinical trial investigator : a step by step guide for developing a clinical trial site / P.K. Julka.
Material type:
TextPublication details: Gurgaon, India : DNA Press, [2009?] Description: 147 p. : ill. ; 22 cmISBN: 9788190827706; 8190827707Subject(s): Biomedical Research -- methods | Drug Discovery | Clinical Trials as TopicNLM classification: W 20.5 2009JUSummary: This book is intended to provide an insight on becoming a successful clinical trial investigator. The book, which would help readers develop a clear understanding on the steps involved in developing a good clinical trial site, has detailed chapters on a variety of important topics, including how to become a clinical trial investigator, how to find and develop clinical trial sites and how to ensure that all procedures adhere to both the law and an organisation's goals and ideals. Each chapter concludes with summary points which will be very helpful for newcomers to the clinical research industry. Additionally, the book ends with useful appendices on essential trial documents, organising informed consent and potential dilemmas researchers may encounter while initiating clinical trials in developing countries like India.
| Item type | Current library | Call number | Copy number | Status | Date due | Barcode |
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WHO HQ BORROWABLE-COLL-STACKS | W 20.5 2009JU (Browse shelf(Opens below)) | 1 | Available | 00081126 |
UNEDITED/Tomas/2011/Dec
This book is intended to provide an insight on becoming a successful clinical trial investigator. The book, which would help readers develop a clear understanding on the steps involved in developing a good clinical trial site, has detailed chapters on a variety of important topics, including how to become a clinical trial investigator, how to find and develop clinical trial sites and how to ensure that all procedures adhere to both the law and an organisation's goals and ideals. Each chapter concludes with summary points which will be very helpful for newcomers to the clinical research industry. Additionally, the book ends with useful appendices on essential trial documents, organising informed consent and potential dilemmas researchers may encounter while initiating clinical trials in developing countries like India.
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