Literature DB >> 21052860

Clinical study reflections: another view: Commentary on: "Raising suspicions with the Food and Drug Administration: detecting misconduct".

Patricia Spitzig1.   

Abstract

Federal regulations are the minimum requirements for conducting clinical studies. Some innovation would improve the situation of many involved in these studies, including: study subjects, those who monitor studies, and clinical investigators as well as Institutional Review Boards. Respecting patient and whistle-blower input; appreciating research staff contributions; and implementing a systems and partnership approach would foster quality and advance clinical research.

Entities:  

Mesh:

Year:  2010        PMID: 21052860     DOI: 10.1007/s11948-010-9235-1

Source DB:  PubMed          Journal:  Sci Eng Ethics        ISSN: 1353-3452            Impact factor:   3.525


  3 in total

1.  Protection of human subjects.

Authors: 
Journal:  Code Fed Regul Shipping       Date:  1982-10-01

2.  Raising suspicions with the Food and Drug Administration: detecting misconduct.

Authors:  Michael R Hamrell
Journal:  Sci Eng Ethics       Date:  2010-09-15       Impact factor: 3.525

3.  Many scientists admit to misconduct: degrees of deception vary in poll; researchers say findings could hurt the field.

Authors:  Rick Weiss
Journal:  Washington Post       Date:  2005-06-09
  3 in total
  1 in total

1.  Editors' overview: topics in the responsible management of research data.

Authors:  Joe Giffels; Sara H Vollmer; Stephanie J Bird
Journal:  Sci Eng Ethics       Date:  2010-10-28       Impact factor: 3.525

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.