Exploring the impact of high shear mixing process parameters on the physical characteristics of excipient powder blend by design of experiments
Kovács, Béla, Tőkés, Erzsébet Orsolya, Kelemen, Éva Katalin, Zöldi, Katalin, Suba, Edit, Kovács-Deák, Boglárka, Székely-Szentmiklósi, István, Boda, Francisc, Casian, Tibor
Development and Validation of an UV-Spectrophotometric Method for the Assay of Strontium Ranelate and HPLC Stability Testing from Bulk and Pharmaceutical Dosage Form
Kovács, Béla, Molnár, Réka, Nagy, Előd Ernő, Kelemen, Éva Katalin, Székely-Szentmiklósi, Blanka, Székely-Szentmiklósi, István, Kovács-Deák, Boglárka, Gyéresi, Árpád
Study of the effect of formulation variables on the characteristics of combination tablets containing enalapril maleate and indapamide as active substances using experimental design
Szabó, Zoltán-István, Székely-Szentmiklósi, Blanka, Deák, Boglárka, Székely-Szentmiklósi, István, Kovács, Béla, Zöldi, Katalin, Sipos, Emese
Quality-by-design in pharmaceutical development: From current perspectives to practical applications
Kovács, Béla, Péterfi, Orsolya, Kovács-Deák, Boglárka, Székely-Szentmiklósi, István, Fülöp, Ibolya, Bába, László-István, Boda, Francisc
HPLC method development for fampridine using Analytical Quality by Design approach
Kovács, Béla, Boda, Francisc, Fülöp, Ibolya, Székely-Szentmiklósi, István, Kelemen, Éva Katalin, Kovács-Deák, Boglárka, Székely-Szentmiklósi, Blanka