Zobrazeno 1 - 7
of 7
pro vyhledávání: '"критерії прийнятності"'
Publikováno v:
ScienceRise: Pharmaceutical Science; № 6 (28) (2020); 56-67
Aim. The paper intends to frame and pilot the optimised science-based principles of the assay transfer.Materials and methods. The research was performed on desloratadine film-coated tablets, using an analytical balance Mettler Toledo XP 205DR and Cla
Publikováno v:
ScienceRise: Pharmaceutical Science; № 5 (27) (2020); 43-51
Aim. The work aimed at metrological evaluation and management of the risk of inconsistency in the results of desloratadine assay in film-coated tablets.Materials and methods. A pilot-scale batch of the pharmaceutical preparation Alerdez served as a s
Publikováno v:
ScienceRise: Pharmaceutical Science, Vol 0, Iss 1 (11), Pp 16-20 (2018)
The study of dissolution profiles is important as a cheap and easy supplement to bioequivalence research, and as a variation to such studies. This method is not outlined in the State Pharmacopoeia of Ukraine for the doxycycline capsules. Therefore, a
Publikováno v:
ScienceRise: Pharmaceutical Science, Vol 0, Iss 2 (2), Pp 42-45 (2016)
Забезпечення якості результатів випробувань є одним із актуальних питань діяльності контрольно-аналітичних лабораторій. За результат
Publikováno v:
ScienceRise: Pharmaceutical Science; № 1 (11) (2018); 16-20
The study of dissolution profiles is important as a cheap and easy supplement to bioequivalence research, and as a variation to such studies. This method is not outlined in the State Pharmacopoeia of Ukraine for the doxycycline capsules. Therefore, a
Publikováno v:
Фармацевтичний часопис, Vol 0, Iss 4 (2017)
The aim of the work. Providing the documentary evidence, which will confirm that «Uronefron» manufacturing process in the form of film-coated tablets yields the manufacture of the product with the established quality. Materials and Methods. Validat
Publikováno v:
ScienceRise: Pharmaceutical Science; № 2 (2) (2016); 42-45
Quality assurance of test results is one of the topical issues of analytical laboratories functioning. Scientifically reasonable criteria and recommendations in relation to the scheme and quality control of pharmacopoeial tests results by volumetric