|
[Related PubMed/MEDLINE]
Total Number of Papers: 39
|
|
|
| |
|
[Entries Per Page]
|
|
per page
|
| |
|
Page Control
|
|
|
| Page: of |
|
|
|
| No. |
Year |
Title |
Co-occurring Abbreviation |
| 1 |
2019 |
Clinical ethics consultation among Italian ethics committee: Amixed method study. |
EU |
| 2 |
2019 |
Huge variation in obtaining ethical permission for a non-interventional observational study in Europe. |
EA, IRBs, NCs |
| 3 |
2019 |
Implications of product withdrawal on a post-approval pragmatic trial: The VOLUME study experience. |
DMC, IRB, PCT, SSC |
| 4 |
2018 |
Compassionate use programs in Italy: ethical guidelines. |
CU, CUP |
| 5 |
2018 |
Design characteristics of the Corrona Japan rheumatoid arthritis registry. |
RA |
| 6 |
2018 |
Effects of selexipag and its active metabolite in contrasting the profibrotic myofibroblast activity in cultured scleroderma skin fibroblasts. |
alpha-SMA, ECM, FN, SSc |
| 7 |
2018 |
Managing conflict of interest in Ethics Committee. |
COI |
| 8 |
2018 |
The views of ethics committee members and medical researchers on the return of individual research results and incidental findings, ownership issues and benefit sharing in biobanking research in a South Indian city. |
--- |
| 9 |
2017 |
"The invisible": Participant's experiences in clinical trials. |
CROs |
| 10 |
2017 |
Cochrane Collaboration Systematic Reviews may be based on trials not approved by a research ethics committee. |
IRB, SR |
| 11 |
2017 |
Ethics Committees in India: Past, present and future. |
CTRI |
| 12 |
2017 |
Ethics of Safety Reporting of a Clinical Trial. |
ADR, AE, SAE |
| 13 |
2017 |
Ford and Edison in a modern regulatory environment: the first-in-human trial of night-work and artificial light. |
FDA |
| 14 |
2016 |
A Study of Assessing Errors and Completeness of Research Application Forms Submitted to Instituitional Ethics Committee (IEC) of a Tertiary Care Hospital. |
IEC, IRB |
| 15 |
2016 |
Expanded Access Programme: looking for a common definition. |
EAP, EMA, FDA |
| 16 |
2016 |
Potential Risks and Mitigation Strategies Before the Conduct of a Clinical Trial: An Industry Perspective. |
CDA, CRC, CRF, CTA, ICF, SRF |
| 17 |
2016 |
Profile of Institutional Ethics Committees in Dental Teaching Institutions in Kerala, India. |
IECs |
| 18 |
2015 |
Awareness about Ethics Committee amongst the Medical Teachers in a Medical College. |
--- |
| 19 |
2015 |
Conflict of interest in clinical research. |
--- |
| 20 |
2014 |
Research ethics committees: Need for harmonization at the national level, the global and Indian perspective. |
--- |
| 21 |
2013 |
Feasibility study of clinical trial for breast cancer and lung cancer at Indian sites. |
GCP |
| 22 |
2013 |
[Evaluation of the written informed consent form in clinical trials]. |
WICF |
| 23 |
2012 |
A study to assess completeness of project application forms submitted to Institutional Ethics Committees (IEC) of a tertiary care hospital. |
IEC |
| 24 |
2012 |
Ethics committees in India: Facing the challenges! |
--- |
| 25 |
2012 |
Functions and outcomes of a clinical medical ethics committee: a review of 100 consults. |
LST, PCCS |
| 26 |
2012 |
Post-trial access to study medication: a Brazilian e-survey with major stakeholders in clinical research. |
--- |
| 27 |
2012 |
Reporting of ethical committee approval and patient consent in the Portuguese Journal of Pulmonology and in the other Portuguese medical journals with impact factor. |
--- |
| 28 |
2010 |
[Research Ethics Committees in Abruzzo: criticisms and prospects for developments]. |
--- |
| 29 |
2009 |
Ethical bodies: are they possible under democratic systems? The Turkish example. |
--- |
| 30 |
2009 |
Profile and role of the members of ethics committees in hospitals and research organisations in Pune, India. |
--- |
| 31 |
2008 |
[Obtaining medical ethical approval for a multicentre, randomised study: prospective evaluation of a ponderous process]. |
--- |
| 32 |
2006 |
Scientific research on human subjects and ethics procedures at the Istituto Superiore di Sanita: a survey of the articles issued in 2001. |
IC, ISS |
| 33 |
2006 |
Some methodological aspects of ethics committees' expertise: the Ukrainian example. |
--- |
| 34 |
2005 |
[Functioning of hospital Ethics Committee before and after entry in force of new Royal Decree 223/2004 on Clinical Trials with Drugs]. |
RD |
| 35 |
2004 |
Adaptation of the clinical trials directive: recommendations on the contents of a dossier for the request for authorisation of the first trials in human subjects. |
CPP, ICH, IMP |
| 36 |
2003 |
Ethics committees in Italy: a survey on a sample of oncologists. |
--- |
| 37 |
2002 |
Are gastroenterologists aware of the role of ethics committees? |
--- |
| 38 |
1999 |
Conducting clinical trials in Singapore. |
GCP, MCRC |
| 39 |
1999 |
[Ethical dilemmas in gastroenterology practice in Latin-American countries: the AIGE survey]. |
AIGE |
|
A Search Service for Abbreviation / Long Form
