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Srovnatelnost testových verzí slovenské maturitní zkoušky z anglického jazyka
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Year: 2021 Publisher: Brno : Masaryk University Press,

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Title in English: Test versions equivalence of the Slovak upper-secondary school leaving examination The research presented in this book strives to answer how test versions equivalence - a necessary condition for meaningful and fair interpretation and comparison of students' results - could be achieved in the context of high-stakes examination. The research was carried on the Slovak upper-secondary school leaving examination in English at B1 level, namely on the tests of receptive skills operationalized between 2012 and 2015. Theoretical research on the methods and procedures and the application of some of them on the Slovak examinations in the empirical part provided deep insight into the degree of comparability of the test versions used between 2012 and 2015 and made it possible to identify problem areas in terms of test versions comparability. The research helped to identify suitable methods and approaches that might enable to develop equivalent test versions and subsequently, to interpret meaningfully the test results and the measured construct, i.e. students' language proficiency.


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Guidance for industry : statistical approaches to establishing bioequivalence.
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Year: 2001 Publisher: Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research,

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Guidance for industry : food-effect bioavailability and fed bioequivalence studies.
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Year: 2002 Publisher: Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research,

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Physician's 1991 drug handbook.
ISBN: 0874343259 9780874343250 Year: 1991 Publisher: Springhouse Springhouse Corp.

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Guidance for industry : submission of summary bioequivalence data for ANDAs.
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Year: 2009 Publisher: Silver Spring, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research,

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Guidance : topical dermatologic corticosteroids, in vivo bioequivalence.
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Year: 1995 Publisher: Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration,

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Guidance for industry : clozapine tables, in vivo bioequivalence and in vitro dissolution testing.
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Year: 2005 Publisher: Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research,

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Guidance for indusry : bioavailability and bioequivalence studies for nasal aerosols and nasal sprays for local action.
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Year: 2003 Publisher: Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research,

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Guidance for industry : nonsterile semisolid dosage forms : scale-up and postapproval changes : chemistry, manufacturing, and controls : in vitro release testing and in vivo bioequivalence documentation.
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Year: 1997 Publisher: Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research,

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Guidance for industry : waiver of in vivo bioavailability studies for immediate-release soild oral dosage forms based on a biopharmaceutics classification system.
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Year: 2000 Publisher: Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research,

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