Examples of using Study protocol in English and their translations into Spanish
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Official
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Colloquial
Who has reviewed the Study Protocol?
The study protocol is accessible here(PDF 790KB).
Does she feel the plaintiff complied with the study protocol?
The study protocol is accessible here(PDF 790KB).
Are unable to adhere to the study protocol for any reason.
The study protocol was registered in ClinicalTrials.
N” stands for a number,which varies depending on the study protocol.
Include the study protocol, amendments and final report.
Alejandro is going to tell us on this occasion a very requested study protocol.
Contact us about your study protocol and site feasibility.
The study protocol was approved by the Ethic Committee of Inonu University.
The first thing is to know some general considerations,then the study protocol.
We propose a study protocol for newborns with known risk factors.
Examinations, tests, blood samples described in the study protocol.
The study protocol consisted of a gradual increase in workload(50%-100%);
In this blog we summarize the SPIRIT statement a powerfull tool to ensure the appropiate content in our study protocol.
The study protocol was approved by the Madrid Clinical Research Ethics Committee.
Per Food and Drug Administration(FDA) regulations and the study protocol, the BrainGate device was removed from him after approximately one year.
The study protocol and consent forms were reviewed and approved by Copernicus Group IRB Protocol HI001.
Title: Development of ultrasound study protocol to establish cardiovascular risk in Pediatrics.
A study protocol to evaluate the feasibility and acceptability of WC/rBS in stable refugee camps was prepared and carried out in Uganda during 1997.
Overseeing progress of the clinical trial to ensure the study protocol is being followed and complies with GCP and ISO 14155.
Study protocol(with version and date): any protocol format can be presented, providad that it contains the sections described in the model that we propose below.
Six to eight paid data collectors attended a full day training on how to implement the study protocol immediately before each data collection period.
The study protocol was reported to be a pilot study, using one dose(10 mg/kg bw/d) in 10 to 15 female Sprague- Dawley rats, which was selected in dose response studies as maximum tolerable dose.
Preliminary study with the objective of determining whether a programme,procedure or study protocol is practicable, as well as finding out data to help in determining the sample size for a definitive study. .
In June 2016, the FDA authorised blood screening for the Zika virus using NAT technology developed by Grifols and Hologic,for use in the United States through the agency's study protocol for investigational new drugs IND.
Initial application, on a small scale, of a study protocol, with the aim of checking whether the design is appropriate, establishing its viability or obtaining information to determine the sample size for the definitive study. .
The intent of conducting a device clinical trial audit is to ensure the capture, analysis andreporting of data in accordance with the study protocol, GCP, regulatory requirements and Standard Operating Procedures SOPs.
The main documentation needed in these two applications is similar: the study protocol, the patient information sheet(PIS) and informed consent(IC), a set of local documents signed by site staff(suitability of facilities, CV of principal investigators), the study XML file generated by the EudraCT website, and documents related to the study drugs.