Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 12 of 528 entries
Sorted by: Best Match Show Resources per page
Biocrimes, microbial forensics, and the physician.

PLoS medicine

Schutzer SE, Budowle B, Atlas RM.
PMID: 16167845
PLoS Med. 2005 Dec;2(12):e337. doi: 10.1371/journal.pmed.0020337. Epub 2005 Sep 27.

No abstract available.

Ethical challenges in international HIV prevention research.

Accountability in research

MacQueen KM, Shapiro K, Karim QA, Sugarman J.
PMID: 15341046
Account Res. 2004 Jan-Mar;11(1):49-61. doi: 10.1080/08989620490280230.

Members of an HIV-prevention research network were asked to describe ethical challenges faced in their work. Major themes included acceptable standards of care for participants, defining research of relevance to host countries, reducing risks related to stigma, designing research...

Assessing ethics of trials in systematic reviews.

BMJ (Clinical research ed.)

Weingarten MA, Paul M, Leibovici L.
PMID: 15105330
BMJ. 2004 Apr 24;328(7446):1013-4. doi: 10.1136/bmj.328.7446.1013.

No abstract available.

Informed consent in research involving human subjects.

The Journal of clinical ethics

Li BF.
PMID: 15202355
J Clin Ethics. 2004;15(1):35-7.

No abstract available.

Shadowing physicians.

JAMA

Teitz CC.
PMID: 21673291
JAMA. 2011 Jun 15;305(23):2414; author reply 2415-6. doi: 10.1001/jama.2011.787.

No abstract available.

[Preparation of patients scheduled for inguinal hernia surgery].

MMW Fortschritte der Medizin

Braun C, Imdahl A.
PMID: 17615716
MMW Fortschr Med. 2007 Jan 25;149(4):37-8. doi: 10.1007/BF03364933.

In principle, hernias should always be managed surgically. In the event of an acute incarceration, the patient must be referred to hospital immediately, since the condition is lifethreatening. The decision as the type of surgical procedure is made on...

Challenges in the evaluation, consent, ethics and history of early clinical trials - Implications of the Tuskegee 'trial' for safer and more ethical clinical trials.

Current opinion in molecular therapeutics

Lowenstein PR, Lowenstein ED, Castro MG.
PMID: 19806495
Curr Opin Mol Ther. 2009 Oct;11(5):481-4.

No abstract available.

Is the clinical advice you give your patients evidence-based?.

Medscape journal of medicine

Clancy C.
PMID: 19099002
Medscape J Med. 2008;10(11):252. Epub 2008 Nov 03.

No abstract available.

Effective use of consent forms and interactive questions in the consent process.

IRB

Palmer BW, Cassidy EL, Dunn LB, Spira AP, Sheikh JI.
PMID: 18512654
IRB. 2008 Mar-Apr;30(2):8-12.

No abstract available.

[Evaluation and improvement of the management of informed consent in the emergency department].

Revista de calidad asistencial : organo de la Sociedad Espanola de Calidad Asistencial

del Pozo P, García JA, Escribano M, Soria V, Campillo-Soto A, Aguayo-Albasini JL.
PMID: 19717079
Rev Calid Asist. 2009 Sep-Oct;24(5):222-7. doi: 10.1016/j.cali.2009.01.001. Epub 2009 Jul 23.

OBJECTIVE: To assess the preoperative management in our emergency surgical service and to improve the quality of the care provided to patients.MATERIAL AND METHODS: In order to find the causes of non-compliance, the Ishikawa Fishbone diagram was used and...

'Never heard of it'- understanding the public's lack of awareness of a new electronic patient record.

Health expectations : an international journal of public participation in health care and health policy

Bratan T, Stramer K, Greenhalgh T.
PMID: 20579117
Health Expect. 2010 Dec;13(4):379-91. doi: 10.1111/j.1369-7625.2010.00608.x.

BACKGROUND: The introduction of electronic patient records that are accessible by multiple providers raises security issues and requires informed consent - or at the very least, an opportunity to opt out. Introduction of the Summary Care Record (SCR) (a...

When should re-consent of subjects participating in a clinical trial be requested? A case-oriented algorithm to assist in the decision-making process.

Clinical pharmacology and therapeutics

Dal-Ré R, Avendaño C, Gil-Aguado A, Gracia D, Caplan AL.
PMID: 17882160
Clin Pharmacol Ther. 2008 May;83(5):788-93. doi: 10.1038/sj.clpt.6100357. Epub 2007 Sep 19.

Investigators, sponsors, and institutional review boards have to decide when re-consent of clinical trials' participants must be obtained when new information becomes available. We present an algorithm to help in the decision-making process, which takes into consideration the kind...

Showing 1 to 12 of 528 entries