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Four reasons why too many informed consents to clinical research are invalid: a critical analysis of current practices.
Not available
S-EPMC8900041
|
biostudies-literature
Cite
A patient-centred web-based adverse drug reaction reporting system identifies not yet labelled potential safety issues.
Not available
S-EPMC8212270
|
biostudies-literature
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Prognostic factors for overall survival in patients with chronic myeloid leukemia treated with imatinib at the National Cancer Institute - Mexico, from 2000 to 2016.
Not available
S-EPMC6558595
|
biostudies-literature
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Blood draws up to 3% of blood volume in clinical trials are safe in children.
Not available
S-EPMC6587985
|
biostudies-literature
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Challenges and proposed solutions in making clinical research on COVID-19 ethical: a status quo analysis across German research ethics committees.
Not available
S-EPMC8287116
|
biostudies-literature
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Correct use of non-indexed eGFR for drug dosing and renal drug-related problems at hospital admission.
Not available
S-EPMC7661404
|
biostudies-literature
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Utilisation and off-label prescriptions of respiratory drugs in children.
Not available
S-EPMC4152124
|
biostudies-literature
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Tiotropium Respimat(®) vs. HandiHaler(®): real-life usage and TIOSPIR trial generalizability.
Not available
S-EPMC4833170
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biostudies-literature
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Time trends of period prevalence rates of patients with inhaled long-acting beta-2-agonists-containing prescriptions: a European comparative database study.
Not available
S-EPMC4338187
|
biostudies-literature
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Oral insulin immunotherapy in children at risk for type 1 diabetes in a randomised controlled trial.
Not available
S-EPMC8012335
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biostudies-literature
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