Unosi

• Ispitivanje mikrobiološkog i fizičko-hemijskog kvaliteta destilovane vode (2019-10)

  N. Okuka, Ž. Gagić, I. Kasagić-Vujanović, Ispitivanje mikrobiološkog i fizičko-hemijskog kvaliteta destilovane vode, Knjiga sažetaka, pp. 342 - 343, Oct, 2019

• IQPharm organizing committee member for the introductory simpozium "Advancing pharmacy trough education in Bosnia and Herzegovina" (ERASMUS+) Sarajevo (2021-07)

  I. Kasagić-Vujanović, IQPharm organizing committee member for the introductory simpozium "Advancing pharmacy trough education in Bosnia and Herzegovina" (ERASMUS+) Sarajevo, Jul, 2021

• Uticaj kiselinskog izdvajanja aluminijuma na nano-strukturna svojstva termički tretiranog pirofilita iz nalazišta Parsovići (2020-07-24T13:21:39.656Z)

• Hemometrijska analiza hromatografskog ponašanja amlodipin-besilata i bisoprolol-fumarata u tečnoj hromatografiji hidrofilnih interakcija (2016)

• Farmakopeja Bosne i Hercegovine - Nacionalni dodatak Evropskoj farmakopeji (2022)

  A. Uzunović, A. Borić, I. Kasagić-Vujanović, B. Gojić, J. Bešić-Kurteš, D. Kovčić, K. Durić, L. Semizović, i ostali, Farmakopeja Bosne i Hercegovine - Nacionalni dodatak Evropskoj farmakopeji, AGENCIJA ZA LIJEKOVE I MEDICINSKA SREDSTVA BOSNE I HERCEGOVINE, 2022

• Monitoring of bisoprolol fumarate stability under different stress conditions (2017-03)

  I. Kasagić-Vujanović, Monitoring of bisoprolol fumarate stability under different stress conditions, STED Journal, Vol. 1, pp. 415 - 424, Mar, 2017

• Testing of the influence of media's pH value on the solubility and partition coefficient of the acetylsalicylic acid (2017-03)

  D. Knežević, I. Kasagić-Vujanović, Testing of the influence of media's pH value on the solubility and partition coefficient of the acetylsalicylic acid, STED Journal, Vol. 1, pp. 368 - 371, Mar, 2017

• Farmakopejske metode u kontroli kvaliteta lijekova (2021)

  I. Kasagić-Vujanović, Farmakopejske metode u kontroli kvaliteta lijekova, Medicinski fakultet Univerziteta u Banjoj Luci, 2021

• Testiranje robusnosti metode tečne hromatografije za određivanje itrakonazola i njegovih nečistoća primenom frakcionog faktorskog dizajna (2012-02)

  I. Kasagić-Vujanović, M. Jovanović, T. Rakić, B. Jančić Stojanović, D. Ivanović, Testiranje robusnosti metode tečne hromatografije za određivanje itrakonazola i njegovih nečistoća primenom frakcionog faktorskog dizajna, Arhiv za farmaciju, Vol. 62, No. 5, pp. 475 - 488, Feb, 2012

• Ispitivanje sadržaja aktivne supstance i degradacionih proizvoda/nečistoća u tabletama nimesulida primjenom reverzno-fazne tečne hromatografije pod visokim pritiskom (2013)

  B. Tubić, I. Vujanović-Kasagić, N. Mihajlica, Ž. Gagić, N. Bubić Pajić, Ispitivanje sadržaja aktivne supstance i degradacionih proizvoda/nečistoća u tabletama nimesulida primjenom reverzno-fazne tečne hromatografije pod visokim pritiskom, Arhiv za farmaciju, Vol. 63, No. 1, pp. 1 - 19, 2013

• Chemometrically assissted optimization and validation of RP–HPLC method for the analysis of itraconazole and its impurities (2013-06)

  I. Kasagić-Vujanović, A. Malenović, M. Jovanović, T. Rakić, B. Stojanović, D. Ivanović, Chemometrically assissted optimization and validation of RP–HPLC method for the analysis of itraconazole and its impurities, ACTA PHARMACEUTICA, Vol. 63, No. 2, pp. 159 - 173, Jun, 2013

• Studije forsirane degradacije amlodipin-besilata i bisoprolol-fumarata primjenom tečne hromatografije hidrofilnih interakcija (2014)

  I. Kasagić-Vujanović, B. Jančić Stojanović, D. Ivanović, Studije forsirane degradacije amlodipin-besilata i bisoprolol-fumarata primjenom tečne hromatografije hidrofilnih interakcija, Arhiv za farmaciju, Vol. 64, No. 3, pp. 230 - 246, 2014

• Stability study of amlodipine besylate and bisoprolol fumarate in aqueous solutions (2014)

  I. Vujanović-Kasagić, D. Jelić, V. Antunović, B. Jančić-Stojanović, D. Ivanović, Stability study of amlodipine besylate and bisoprolol fumarate in aqueous solutions, CONTEMPORARY MATERIALS, Vol. 5, No. 2, pp. 212 - 221, 2014

• Comparison of full factorial desing, central composite desing and Box Behenken desing in cromatographic method development for the analysis of fluconazole and its impurities (2014-02)

  T. Rakić, I. Kasagić-Vujanović, M. Jovanović, B. Jančić Stojanović, D. Ivanović, Comparison of full factorial desing, central composite desing and Box Behenken desing in cromatographic method development for the analysis of fluconazole and its impurities, ANALYTICAL LETTERS: AN INTERNATIONAL JOURNAL FOR RAPID COMMUNICATION, Vol. 47, No. 8, pp. 1334 - 1347, Feb, 2014

• Desing of experiments in optimization and validation of a hydrophilic interaction liquid chromatography method for determination of amlodipin besylate and bisoprolol fumarate (2015-02)

  I. Kasagić-Vujanović, B. Jančić-Stojanović, T. Rakić, D. Ivanović, Desing of experiments in optimization and validation of a hydrophilic interaction liquid chromatography method for determination of amlodipin besylate and bisoprolol fumarate, Journal of Liquid Chromatography & Related Technologies, Vol. 38, No. 8, pp. 919 - 928, Feb, 2015

• STRESS DEGRADATION OF LISINOPRIL DIHYDRATE IN DIFFERENT AQUEOUS MEDIA (2017-02)

  I. Kasagić-Vujanović, D. Knežević, N. Vukićević, STRESS DEGRADATION OF LISINOPRIL DIHYDRATE IN DIFFERENT AQUEOUS MEDIA, Contemporary Materials, Vol. 2, No. 8, pp. 164 - 171, Feb, 2017

• Investigation of the retention mechanisms of amlodipine besylate, bisoprolol fumarate, and their impurities on three different HILIC columns (2018-10)

  I. Kasagić-Vujanović, B. Jančić-Stojanović, D. Ivanović, Investigation of the retention mechanisms of amlodipine besylate, bisoprolol fumarate, and their impurities on three different HILIC columns, JOURNAL OF LIQUID CHROMATOGRAPHY AND RELATED TECHNOLOGIES, Vol. 41, No. 9, pp. 523 - 531, Oct, 2018

• Quality control of distilled water used for reconstitution of powders for oral suspension in pharmacies on the territory of Bosnia and Herzegovina (2019)

  I. Kasagić-Vujanović, Ž. Gagić, N. Okuka, D. Knežević, Quality control of distilled water used for reconstitution of powders for oral suspension in pharmacies on the territory of Bosnia and Herzegovina, CONTEMPORARY MATERIALS, Vol. X, No. 1, pp. 47 - 55, 2019

• Quality by Design oriented development of hydrophilic interaction liquid chromatography method for the analysis of amitriptyline and its impurities (2019-05)

  I. Kasagić-Vujanović, B. Jančić-Stojanović, Quality by Design oriented development of hydrophilic interaction liquid chromatography method for the analysis of amitriptyline and its impurities, JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, Vol. 173, pp. 86 - 95, May, 2019

• Design of experiments in optimization and validation of hydrophilic interaction liquid chromatography method for determination of amlodipine besylate and its impurities (2020)

  I. Kasagić-Vujanović, D. Knežević, Design of experiments in optimization and validation of hydrophilic interaction liquid chromatography method for determination of amlodipine besylate and its impurities, Acta Chromatographica , Vol. AChrom 2021;, pp. 1 - 12, 2020