Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Ravindra B Ghooi"'
Autor:
Ravindra B Ghooi
Publikováno v:
Perspectives in Clinical Research, Vol 6, Iss 1, Pp 10-14 (2015)
Increased focus on ethical review of research demands a number of improvements in the existing system. Although these are being implemented, some factors that have received less attention in the past could be examined. One of these is conflict of int
Externí odkaz:
https://doaj.org/article/aa01ce14641f4d8ba7ef7810eb5a534c
Autor:
Ravindra B Ghooi, Deepa Divekar
Publikováno v:
Perspectives in Clinical Research, Vol 5, Iss 4, Pp 145-150 (2014)
Aims and Objectives: Sponsors need to pay for management of all serious adverse events suffered by subjects in a clinical trial and to compensate for injuries or deaths related to the trial. This study examines if insurance policies of trials, cover
Externí odkaz:
https://doaj.org/article/a49be73dbd64490885c6431dbad96346
Autor:
Ravindra B Ghooi
Publikováno v:
Perspectives in Clinical Research, Vol 5, Iss 2, Pp 60-65 (2014)
Institutional Review Boards (IRBs) are an important link in subject protection program, and their function defines ethical credentials of research. Of late there has been a furore in the country over the number of deaths in clinical research, and all
Externí odkaz:
https://doaj.org/article/164f5651d77e4e05bd24af5036613ad3
Autor:
Ravindra B Ghooi
Publikováno v:
Perspectives in Clinical Research, Vol 4, Iss 4, Pp 199-203 (2013)
Three amendments to the drugs and cosmetics rules were published in quick succession in 2013. These addressed the issues of compensation of injury and death in clinical trials in addition to the role and registration of Ethics Committees. Of the thre
Externí odkaz:
https://doaj.org/article/9e72dfe7b5b444e485d1f2088b80097d
Autor:
Ravindra B Ghooi
Publikováno v:
Perspectives in Clinical Research, Vol 2, Iss 2, Pp 72-76 (2011)
The Nuremberg Code drafted at the end of the Doctor′s trial in Nuremberg 1947 has been hailed as a landmark document in medical and research ethics. Close examination of this code reveals that it was based on the Guidelines for Human Experimentatio
Externí odkaz:
https://doaj.org/article/dbb4595de529446fb7f770daa28f7cc1
Autor:
Ravindra B Ghooi
Publikováno v:
Perspectives in Clinical Research, Vol 5, Iss 1, Pp 3-5 (2014)
The voluntary consent of a subject participating in research is fundamental to the principle of autonomy. This consent must be free from any coercion, intimidation, falsehood, physical, psychological, or economic pressure. It is in the interest of th
Externí odkaz:
https://doaj.org/article/d9fbd8673a5e487ca1ff7337c38498b8
Autor:
Ravindra B Ghooi
Publikováno v:
Perspectives in Clinical Research, Vol 1, Iss 4, Pp 139-142 (2010)
Clinical research institutions have mushroomed in the country, though there is a generalized lack of experienced faculty. These institutes mostly confine themselves to theoretical aspects of clinical research, since there is lack of facilities for pr
Externí odkaz:
https://doaj.org/article/4133a9d559ab45c1af45af917f5385a3
Autor:
Ravindra B Ghooi
Publikováno v:
Perspectives in Clinical Research, Vol 7, Iss 3, Pp 109-110 (2016)
Externí odkaz:
https://doaj.org/article/84e50759a6b74f09a03136cfa8feaf78
Autor:
Ravindra B Ghooi
Publikováno v:
Perspectives in Clinical Research, Vol 6, Iss 3, Pp 123-124 (2015)
Externí odkaz:
https://doaj.org/article/d79ff51b58a04759adfeaf03191e0f30
Autor:
Ravindra B. Ghooi
Publikováno v:
Journal of Ayurveda and Integrative Medicine, Vol 13, Iss 3, Pp 100564- (2022)
Externí odkaz:
https://doaj.org/article/0e0f79a0d4154c6a9573f9a29bf7599a