Examples of 'all clinical trials' in a sentence
Meaning of "all clinical trials"
The phrase 'all clinical trials' refers to the complete set of studies or investigations conducted to test the effectiveness, safety, and potential side effects of new drugs, medical treatments, or procedures. Clinical trials are crucial in the development and approval process of medical interventions. They involve carefully designed protocols, ethical considerations, and rigorous data collection to evaluate the impact and viability of a specific intervention on human subjects
How to use "all clinical trials" in a sentence
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all clinical trials
All clinical trials involve risk to participants.
A tabulae pcesentation of all clinical trials should be given.
Not all clinical trials have a control group.
A protocol is a study on which all clinical trials are based.
Not all clinical trials are expensive.
This is a general issue for all clinical trials.
All clinical trials are recorded in a registry accessible to the public.
Access to all clinical trials.
All clinical trials have the potential to produce AEs.
Coordinates all clinical trials.
All clinical trials have specific guidelines for participant eligibility.
An ethics board must grant approval to all clinical trials.
A tabular presentation of all clinical trials and studies should be given.
All clinical trials are designed to be as safe as possible for the participants.
Patient safety is a priority in all clinical trials for neck pain.
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All clinical trials are voluntary and information collected during them is confidential.
Regulatory bodies require data on SAEs to be collected in all clinical trials.
All clinical trials are exposed to the same procedure by this directive.
This web application is suitable for all clinical trials specification.
All clinical trials with dasabuvir have been conducted following administration with food.
Not all men are eligible for all clinical trials.
Adverse reactions from all clinical trials are listed according to the following frequency.
Route of administration has been used for oritavancin in all clinical trials to date.
All clinical trials have criteria specifying who can or can not participate.
Rare cases of pancreatitis have been reported from a review of all clinical trials with quetiapine.
All clinical trials feature guidelines about who may or may not participate.
This database contains information on all clinical trials performed in the EU.
All clinical trials are conducted in compliance with stringent scientific and ethical principles.
This guarantees the quality of all clinical trials carried out at the Centre.
Half of all clinical trials fail in their objective to meet the quantitative sampling target.
Member States should efficiently assess all clinical trials applications within the given timelines.
All clinical trials have rules about who can and can not participate.
IRBs approve and monitor almost all clinical trials in the United States.
All clinical trials relevant to clinical efficacy evaluation were performed using probenecid concomitantly with cidofovir.
It oversees and regulates phases I through III of all clinical trials conducted in Canada.
All clinical trials are conducted in the same centres that provide standard treatment for cancer.
Individual results may vary from individual to individual, as is seen in all clinical trials.
All clinical trials should be registered in the EU database prior to being started.
Figure 1 depicts the forest plot of all clinical trials included in this meta-analysis.
All clinical trials were approved by the local Medical Ethical Committee.
Alpha-GPC was safe in all clinical trials.
The FDA reviews all clinical trials that use new medicine or other treatments.
OpenTrials, towards a collaborative open database of all available information on all clinical trials.
In the past, almost all clinical trials were done at cancer centers.
All clinical trials applications will be reviewed by the appropriate sub-Committee.
It 's a given because all clinical trials in Canada need REB approval.
All clinical trials should be registered with a recognized and easily webaccessible public registry.7.
In the United States, the FDA must approve all clinical trials involving newly developed pharmaceuticals.
All clinical trials with ombitasvir, paritaprevir and ritonavir have been conducted following administration with food.
In principle, all clinical trials conducted in Switzerland must.
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