dokument informiranog pristanka

dokument informiranog pristanka

Dokument koji opisuje prava sudionika u ispitivanju i uključuje detalje o ispitivanju, kao što su njegova svrha, trajanje, zahtijevani postupci i ključni kontakti. Rizici i potencijalne dobrobiti su opisane u dokumentu informiranog pristanka. Sudionici onda odlučuju hoće li ili neće potpisati dokument. Informirani pristanak nije ugovor i sudionik se može u svakom trenutku povući iz ispitivanja.

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Sõnaliik: noun
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Blossary:
Valdkond/domeen: Pharmaceutical
Category: Clinical trials
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Seotud terminid

pristup

Medical devices; Clinical trials

get information from the computer where it is stored

farmakokinetika

Pharmaceutical; Clinical trials

The processes (in a living organism) of absorption, distribution, metabolism, and excretion of a drug or vaccine.

placebo

Pharmaceutical; Clinical trials

A placebo is an inactive pill, liquid, or powder that has no treatment value. In clinical trials, experimental treatments are often compared with placebos to assess the ...

upute za korištenje

Biotechnology; Health care; Life Sciences; Medical; Biochemistry; Biofuel; Biomedical; Behavioral science

"a manual usually accompanying a technical device and explaining how to install or operate it" Essential Requirements - Medical Device Directive 93/42/EEC - Annex I, 13.1: Each ...

opis

Biotechnology; Health care; Life Sciences; Medical; Biochemistry; Biofuel; Biomedical; Behavioral science

description a statement presenting something in words, from verb describe

komplikacije

Biotechnology; Health care; Life Sciences; Medical; Biomedical; Diseases; Hospitals; Diseases

Complication, in medicine, is an unfavorable evolution of a disease, a health condition or a medical treatment. The disease can become worse in its severity or show a higher ...