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протокол

A study plan on which all clinical trials are based. The plan is carefully designed to safeguard the health of the participants as well as answer specific research questions. A protocol describes what types of people may participate in the trial; the schedule of tests, procedures, medications, and dosages; and the length of the study. While in a clinical trial, participants following a protocol are seen regularly by the research staff to monitor their health and to determine the safety and effectiveness of their treatment.

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монтреалски протокол
에너지; 석탄; 천연 가스; 휘발유

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контрола
의약품; 임상시험

A control is the nature of the intervention control.

нежељене реакције
의약품; 임상시험

(Adverse Event.) An unwanted effect caused by the administration of drugs. Onset may be sudden or develop over time (See Side Effects).

заступање и групе за подршку
의약품; 임상시험

Organizations and groups that actively support participants and their families with valuable resources, including self-empowerment and survival tools.

клинички
의약품; 임상시험

Pertaining to or founded on observation and treatment of participants, as distinguished from theoretical or basic science.

клинички истраживач
의약품; 임상시험

A medical researcher in charge of carrying out a clinical trial's protocol.

самилосна употреба
의약품; 임상시험

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