Writing clinical research protocols - Info and Reading Options
ethical considerations
By Evan G DeRenzo
"Writing clinical research protocols" was published by Elsevier Academic in 2006 - Burlington, MA, it has 300 pages and the language of the book is English.
“Writing clinical research protocols” Metadata:
- Title: ➤ Writing clinical research protocols
- Author: Evan G DeRenzo
- Language: English
- Number of Pages: 300
- Publisher: Elsevier Academic
- Publish Date: 2006
- Publish Location: Burlington, MA
“Writing clinical research protocols” Subjects and Themes:
- Subjects: ➤ Clinical trials - Proposal writing in medicine - Human experimentation in medicine - Moral and ethical aspects - Clinical Protocols - Standards - Biomedical Research - Ethics - Clinial trials - Études cliniques - Writing
Edition Specifications:
- Pagination: xix, 300 p. ;
Edition Identifiers:
- The Open Library ID: OL18207725M - OL12350383W
- Online Computer Library Center (OCLC) ID: 62078229 - 56453025
- Library of Congress Control Number (LCCN): 2006282728
- ISBN-10: 0122107519
- All ISBNs: 0122107519
AI-generated Review of “Writing clinical research protocols”:
"Writing clinical research protocols" Table Of Contents:
- 1- Introduction to the art and science of clinical research
- 2- What you need to know about clinical research ethics
- 3- What you need to know about the regulation of clinical research
- 4- Designing a clinical research study
- 5- Selecting subjects for clinical studies
- 6- Risks and benefits in clinical research
- 7- Recruiting subjects
- 8- Informed consent
- 9- Privacy and confidentiality
- 10- The "ethics" section
- 11- Procedures and methods
- 12- Statistics, data collection and management, and record keeping
- 13- Use of human biological materials
- 14- Special issues raised by evolving areas of clinical research
- 15- Case histories : learning from experience
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