Translation of "study protocol design" to Slovene language:
Dictionary English-Slovene
Examples (External sources, not reviewed)
| The overall design of the study was adequately pre specified in the protocol and was considered acceptable. | Celotna zasnova študije je bilo ustrezno predhodno opredeljena v protokolu in je bila sprejemljiva. |
| original VNC encoders and protocol design | prvotni kodirniki VNC in izdelava protokola |
| To submit a descriptive study protocol to CHMP. | Da bo CHMP ju predložil opisni protokol študije. |
| Overall Treatment Success in the Per Protocol Set, Invasive Candidiasis Study | Skupna uspešnost zdravljenja pri posameznem protokolu, študija invazivne kandidoze |
| The study protocol was submitted to the RMS and all CMSs. | Protokol študije je bil predložen referenčni državi članici in vsem zadevnim državam članicam. |
| The experimental design of the study mimicked acute toxic mastitis. | Poskusna zasnova študije je posnemala akutni toksični mastitis. |
| If this study design is feasible and agreed to by the CHMP, EpiCept commits to conduct the study and to aim for a start of recruitment within 1 year of agreement on protocol synopsis and recruitment of 10 patients month. | Če je načrt takšne študije izvedljiv in ga potrdi tudi Odbor za zdravila za uporabo v humani medicini, se družba EpiCept zavezuje, da jo bo izvedla, ter da bo v roku enega leta po sporazumu glede povzetka protokola pričela s sestavljanjem skupine sodelujočih v študiji z naborom 10 bolnikov mesec. |
| HOS Final Protocol Available Patient Enrolment Analysis of Data Immunogenicity Sub study | Preiskava izida Hunterjevega sindroma (Hunter Outcome Survey HOS) |
| The applicant will provide the draft protocol of the study to the CHMP for agreement before study start. | Pred začetkom študije, bo vlagatelj predložil osnutek protokola študije v potrditev CHMP. |
| The experimental design of the study mimics an acute toxic mastitis. | Eksperimentalni načrt raziskave posnema akutni toksični mastitis. |
| (20) 'Protocol' a document that describes the objectives, design, methodology, statistical considerations and organisation of a clinical trial | (20) protokol dokument, ki opisuje cilje, načrt, metodologijo, statistično obdelavo in organizacijo kliničnega preskušanja |
| 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. | Cilj, zasnova in kazalniki izida študije morajo biti v skladu s podobnimi preskušanji, objavljenimi v literaturi, protokol študije pa mora prejeti in potrditi pristojni nacionalni organ referenčne države članice v treh mesecih od odobritve. |
| Final Protocol Available Patient Enrolment Final analysis of Data Under 5 years Sub Study | Končni protokol na voljo Nabor bolnikov Končna analiza podatkov Podštudija do 5 let |
| The study protocol will be finalised and submitted to the EMEA by July 2008. | Protokol študije bo dokončno pripravljen in predložen Evropski agenciji za zdravila do julija 2008. |
| The need to perform a bioequivalence study with the highest strength and a valid study with replicate design was discussed. | Obravnavana je bila potreba po izvedbi bioekvivalenčne študije z največjo jakostjo in veljavne študije na podlagi ponovitvenega načrta. |
| Protective efficacy against cholera in the Bangladesh study (per protocol analysis) Protective efficacy, (95 CI) | Učinkovitost zaščite proti koleri v raziskavi v Bangladešu (analiza po protokolih) Učinkovitost zaščite, (interval zaupanja 95 ) |
| A protocol defined interim analysis (based on 249 TTP events) triggered early study termination for efficacy. | S protokolom določena vmesna analiza (na osnovi 249 TTP dogodkov) je vodila do predčasne prekinitve študije kar zadeva ugotavljanje učinkovitosti. |
| At end of study, subjects enrolled in the two Phase III studies (Protocol 013 and Protocol 015), were followed for up to 4 years (median 3.7 years). | Na koncu študije je bil čas spremljanja oseb, vključenih v dve študiji III. faze (Protokol 013 in Protokol 015), do 4 leta (mediana 3, 7 let). |
| Furthermore, the MAH commits to continue dialogue with EMEA CHMP with regard to study design | Poleg tega se imetnik dovoljenja za promet zavezuje, da se bo v zvezi z nacrtom študije še naprej posvetoval z EMEA CHMP. |
| A technical study should be commissioned to review the current system of boat design categories. | naročilo tehnične študije za pregled sedanjega sistema kategorij namembnosti plovil |
| Per protocol all events on study therapy or within 14 days of discontinuation (excluded patients who took 75 of their study medication or took non study NSAIDs 10 of the time). | Po protokolu (per protocol) vsi dogodki med zdravljenjem v študiji ali v 14 dneh po prekinitvi zdravljenja (bolniki, ki so vzeli 75 zdravila, predvidenega v študiji, ali so 10 časa jemali NSAR e, ki niso bili predvideni v študiji, so izključeni). |
| Protocol is a Filter Protocol | Protokol je filtrirni protokol |
| The CVMP concluded that according to current GCP requirements this pivotal study design has many deficiencies. | CVMP je sklenil, da ima ključna raziskava številne pomanjkljivosti po trenutno veljavnih zahtevah iz smernic za dobro klinično prakso. |
| Results of this pilot study were used to design and implement a multi national phase 3 trial. | Rezultati te pilotne študije so bili osnova za načrtovanje in izvedbo multinacionalnega preskušanja faze 3. |
| Considering the design of the study, no conclusions can be drawn from the results of the separate analysis. | Glede na zasnovo študije ni možno narediti zaključkov iz rezultatov ločene analize. |
| Protocol | Protokol |
| Protocol | Protokol |
| Protocol | Protokol |
| Protocol | Protokol |
| Protocol | protokol |
| The results from the study were used to design the pivotal residue study to include time points at 7, 14, 46 and 57 days after the last injection. | Rezultati študije so bili uporabljeni pri določanju časovnih točk zakola 7, 14, 46 in 57 dni po zadnjem injiciranju. |
| The results from the study were used to design the pivotal residue study to include time points at 7, 14, 21 and 27 days after the last injection. | Na podlagi rezultatov študije je bila oblikovana glavna študija izločanja ostankov s časovnimi točkami 7, 14, 21 in 27 dni po zadnjem injiciranju. |
| communication,culture,design,interface design,telecom | communication,culture,design,interface design,telecom |
| AppSocket Protocol | AppSocket Protocol |
| New protocol | Nov protokol |
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