Examples of using Study protocol in English and their translations into Polish
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Medicine
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Computer
Vucelich's study protocol.
Study protocols to be submitted by September.
To submit a descriptive study protocol to CHMP.
Study protocol within 2 months after Commission Decision.
Submission of study protocol with first PSUR.
Efficacy results are presented for the combined analysis of study protocols.
I just needed to reveal her study protocol, and she would have gone to prison.
The study protocol will be finalised and submitted to the EMEA by July 2008.
Additional information about the IMPACT study is available in the IMPACT study protocol, and other study documents, which can be accessed through the restricted area of this site.
The study protocol should be submitted within 3 months of the EC decision.
Interventional trials, as the name itself suggests,need the participants to try a certain type of treatment, to"be tested" under strict and well-defined rules shown in the study protocol.
The study protocol was submitted to the RMS and all CMSs.
Patients in the phase II study who underwent complete resection of giant cell tumour of bone did receive an additional 6 months of treatment following the surgery as per study protocol.
Full study protocols should be submitted before the study start for CHMP review.
Until February 27, we recruited 109% of the total number of patients requiredto complete the study, of which 75% is a group of patients who received all drug administrations foreseen in the study protocol.
Data shall be collected in accordance with a study protocol that shall involve specialised centres and shall be agreed by the Commission.
A study protocol amendment removed the requirement of routine CT scanning during follow up, and so disease status was assessed by the investigator.
The data should be collected in accordance with a study protocol agreed by the Commission that should involve specialised centres of respiratory allergy.
The study protocol shall be agreed with the CHMP prior to the start of the study and the final results(final study report) provided to the CHMP and EMA by June 2016.
This form of surveillance aims to improve the quality and diver-sity of information sources by developing andimplementing standard and rigorous study protocols, using appropriate methods and tools.
A clinical study(Protocol 016) compared the immunogenicity of Silgard in 10- to 15-year-old girls to those in 16- to 23-year-old women.
In the absence of PD, discontinuation of one component of study treatment in the erlotinib+ Avastin arm did not lead to discontinuation of the other component of study treatment as specified in the study protocol.
The clinical study protocol provided for all patients to receive aspirin and a daily maintenance dose of prasugrel. bAny intracranial haemorrhage or any clinically overt bleeding associated with a fall in haemoglobin≥5 g/dL.
Until 15th December 2014, the data were obtained from about 107% of the total number of patients requiredto complete the study, of which 74% is a group of patients who received all drug administrations foreseen in the study protocol.
GMO applicants are required to provide EFSA with specified studies which have to comply with EU/OECD study protocols and be performed under a given quality assurance system(Good Laboratory Practice or ISO) and in accordance with EFSA's guidance for the risk assessment of GMOs.
The Applicant should conduct a post-marketing microbiological study in order to further elucidate the risk for emergence of resistance in the intestinal and upper respiratory microflora associated with thelong-term use of Oracea, and commit to submitting a study protocol within 3 months of approval.
The scope, design and endpoints of the study should be in line with similar trials published in the literature and the study protocol should be validated by and submitted to the National Competent Authority of the Reference Member State within three months of approval.