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The act of signing up participants into a study. Generally this process involves evaluating a participant with respect to the eligibility criteria of the study and going through the informed consent process.

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行业/领域：制药
类别临床试验
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ранији упис

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контрола

制药; 临床试验

A control is the nature of the intervention control.

протокол

制药; 临床试验

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 ...

нежељене реакције

制药; 临床试验

(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

制药; 临床试验

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

клинички

制药; 临床试验

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

клинички истраживач

制药; 临床试验

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

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