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Protocol - University of Colorado Denver
Protocol - University of Colorado Denver

... Co-morbid factors, including smoking, can further alter susceptibility for pneumonia in the setting of AUDs. For example, investigations in animal models have revealed that ciliary dysfunction is compounded in the presence of both alcohol and cigarette smoke compared to either exposure alone(15), su ...
for research purposes
for research purposes

... approval of amendments, report adverse events to the REB, submit annual reports and cooperate with any monitoring activities determined by the REB. 3. OTHER RESEARCH TEAM MEMBERS WHO ARE NOT CO-INVESTIGATORS (names of individuals who will be accessing personal health information e.g. health records/ ...
6. study procedures
6. study procedures

... which compromises the ethical acceptability of the protocol. This can be a nonmedical event for clinical trials that are not medical or testing drugs or devices, such as those clinical trials conducted in different fields such as psychology. ...
Adverse Event Reporting Requirements
Adverse Event Reporting Requirements

... {It is the policy of the Mary Babb Randolph Cancer Center to strive for gender and minority patient participation that represents the population of West Virginia in all clinical investigations. Between January 2012 and December 2012, 192 patients were enrolled onto clinical trials at the Mary Babb R ...
[ICH E2F] [MODEL DSUR – Non
[ICH E2F] [MODEL DSUR – Non

... artery disease (PAD). In an experimental rabbit PAD model (unilateral femoral artery ligation), we demonstrated that VGF-2 stimulates collateral development through an increase in arteriogenesis (demonstrated with positive bromodeoxyuridine labeling), enhances limb perfusion (fluorescent microsphere ...
Off-Label Paediatric Drug Use for Juvenile Depression and the
Off-Label Paediatric Drug Use for Juvenile Depression and the

... The existence of depression among children has, until quite recently, been regarded as a physiological impossibility by some working within the field of child psychiatry (Freud, 1949; Jones, 1957). Thomas Szasz classically denied the existence of ‘mental illness’ in the 1960s (Szasz, 1960), a claim ...
Research Super User Meeting - Brigham and Women`s Hospital
Research Super User Meeting - Brigham and Women`s Hospital

...  Patient care orders that utilize BWH clinical resources will be entered into Epic ...
$doc.title

... the All8G Snp in response to naltrexone. The conventional approach to a full­ scale outpatient efficacy trial would be to recruit equal numbers of Al18G and wild type subjects and assign them randomly to naltrexone or placebo. However, the relative infrequency of the A118G polymorphism (10-30%) woul ...
TEACHING WRITINGUSING GRAMMAR TRANSLATION METHOD
TEACHING WRITINGUSING GRAMMAR TRANSLATION METHOD

... teaching, definition of teaching, definition writing, definition teaching Writing, C. REASEARCH METHODOLOGY In this part there will be discussed about research design, research method, research population and sample, research instrument. research data collection, research data analyzing, and researc ...
ANOVA one way between
ANOVA one way between

... the top-of-the-line car batteries produced by 3 manufacturers (A, B and C). To provide the database for your assessment, you randomly sample 4 batteries from each manufacturer and run them through laboratory tests that allow you to determine the useful life of each battery. The following are the res ...
intensive bioethics course 2017 - Monash Arts
intensive bioethics course 2017 - Monash Arts

... ABOUT THE PROGRAM ...
Statistical Review and Validation of Patient Narratives
Statistical Review and Validation of Patient Narratives

... Patient profiles present information collected for a subject over the course of a clinical trial that allow a medical writer or reviewer to draft a narrative to coincide with an event of interest. Possible events of interest are commonly serious and or study drug related adverse events, events that ...
19_The_Clinical_Trial_ProcessMini Med_Baquet
19_The_Clinical_Trial_ProcessMini Med_Baquet

... against a particular cancer To see how the agent or intervention affects the human body The dosage found safe in Phase I is used Participants have been treated with chemotherapy, surgery, or radiation, but treatment has not been effective ...
CNM Handbook for Educational Research (doc)
CNM Handbook for Educational Research (doc)

... Administration). It does not include research activities which are incidentally regulated by a federal department or agency solely as part of the department's or agency's broader responsibility to regulate certain types of activities whether research or non-research in nature (for example, Wage and ...
TraCS Institute
TraCS Institute

... reported to IRB within two weeks of the investigator becoming aware of the event.  All SERIOUS unanticipated problems and adverse events will be reported within one week of the investigator becoming aware of the event.  Upon review of the report, the IRB will make a final determination as to wheth ...
November 10, 1998: This is a staff draft report developed... Commission.  It does not represent conclusions and should not...
November 10, 1998: This is a staff draft report developed... Commission. It does not represent conclusions and should not...

... federal regulations. Thus, if a pathology laboratory saves some tissue left over from a clinical ...
UH/NJMS Clinical Research Study Initiation Form
UH/NJMS Clinical Research Study Initiation Form

... For consideration of Medicare payment of CATEGORY B DEVICES and ROUTINE COSTS of ...
Hier steht ein Titel. Dieser Titel kann auch drei Zeilen
Hier steht ein Titel. Dieser Titel kann auch drei Zeilen

... 2.2. RESEARCH ON THE BRAIN AND RELATED DISEASES, HUMAN DEVELOPMENT AND AGEING ...
A PLACEBO-CONTROLLED, MULTICENTER, DOUBLE
A PLACEBO-CONTROLLED, MULTICENTER, DOUBLE

... Literature reports suggest increasing levels of cCK18/M30 were associated with increasing hepatic disease severity and that the higher the cCK18/M30 level, the worse the patient outcome. This study confirmed that ACLF patients had elevated levels of all 3 biomarkers (cCK18/M30, flCK18/M65, Caspase 3 ...
An Exploration of Ethical Issues - ScholarWorks@GVSU
An Exploration of Ethical Issues - ScholarWorks@GVSU

... Study. The study was held from 1932 to 1972 and was composed of 400 impoverished African American men who suffered from latent and tertiary syphilis. Its purpose was to examine the effects of untreated syphilis on longevity and health. However, participants were deceived by the researchers. They wer ...
Presentación de PowerPoint
Presentación de PowerPoint

... It provides a practical language for mediating between developments in science and popular culture and a means for our society to talk about its deepest moral concerns, fears and hopes. This languageis employed to promote scholarly and public understanding of the ethical, legal, social and public po ...
Research - West Suffolk NHS Foundation Trust
Research - West Suffolk NHS Foundation Trust

... Phase I (safety and tolerability) trials which involve first human exposure to a therapeutic agent. Phase II clinical trials primarily are intended to demonstrate whether or not the new drug will provide any benefit and whether that benefit is sufficiently better than standard treatments to warrant ...
40_Krittaecho Siripassorn
40_Krittaecho Siripassorn

... – Timeliness of IRB reviewing procedure – Appropriateness of alternative mechanism of IRB reviewing procedure – Protection rights and welfare of individuals – Outbreak investigation/research activities should be in a timely manner to control the disease ...
Human Enhancement
Human Enhancement

... debilitation and illness caused by old age e.g. heart disease and Alzheimer’s disease. They predict that the natural side effect of their research will be the indefinite postponement of death i.e. people might live for 150 or more years. Cybernetics is the study of how something or someone reacts to ...
Medical Research Council of Zimbabwe
Medical Research Council of Zimbabwe

... namely respect for persons, beneficence and justice. It is generally agreed that these principles, which in the abstract have equal moral force, guide the conscientious preparation of proposals for scientific studies. In varying circumstances they may be expressed differently and given different mor ...
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Human subject research

Human subject research is systematic, scientific investigation that can be either interventional (a ""trial"") or observational (no ""test article"") and involves human beings as research subjects. Human subject research can be either medical (clinical) research or non-medical (e.g., social science) research. Systematic investigation incorporates both the collection and analysis of data in order to answer a specific question. Medical human subject research often involves analysis of biological specimens, epidemiological and behavioral studies and medical chart review studies. (A specific, and especially heavily regulated, type of medical human subject research is the ""clinical trial"", in which drugs, vaccines and medical devices are evaluated.) Human subject research in the social sciences often involves surveys, questionnaires, interviews, and focus groups.Human subject research is used in various fields, including research into basic biology, clinical medicine, nursing, psychology, sociology, political science, and anthropology. As research has become formalized, the academic community has developed formal definitions of ""human subject research"", largely in response to abuses of human subjects.
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